Target identity
Inspection 1253867 · FEI 1783599
Taylor Farms Colorado, Inc. · Colorado Springs, Colorado, United States
Inspection 1253867VAI
Taylor Farms Colorado, Inc.
For Taylor Farms Colorado, Inc., FDA inspection 1253867 (FEI 1783599) ended November 12, 2024 with VAI across 2 project-area rows. The local corpus joins 3 exact citation rows and audits 1 same-FEI Form 483 candidate, including 1 qualifying link. Primary-document observations and independent follow-up remain unverified.
Project areas
2
Citations
3
483 candidates
1
Fiscal year
FY 2025
Inspection classification
Final FDA outcome
VAIVoluntary Action Indicated
FDA found objectionable conditions or practices, but the agency was not prepared to take or recommend administrative or regulatory action. Voluntary correction is expected.
FDA assigns classifications after evaluating the inspection findings and the firm's response or corrective actions. The Inspection Classification Database contains closed inspections with final classifications, but FDA says not every inspection is included.
What this inspection record establishes
Evidence-bounded interpretation
Project-area outcomes
Food Composition, Standards, Labeling and Econ: VAI; Foodborne Biological Hazards: VAI
Every classification is preserved at project-area row level; the headline is a navigation summary only.
Inspected scope
Food Composition, Standards, Labeling and Econ and Foodborne Biological Hazards
Food/Cosmetics · Colorado Springs, Colorado, United States
Exact citations
3 rows · 3 groups
Joined only by exact InspectionID and grouped by normalized provision.
Form 483 candidate audit
1 considered · 1 qualifying
1 high-confidence FEI/date, 0 firm-context, 0 excluded for date conflict.
Primary documents and follow-up
Not verified
No Form 483/EIR text or exact enforcement source has been reviewed, so observations and actions are not inferred.
Project areas
Per project area
- VAI
Food Composition, Standards, Labeling and Econ
Food/Cosmetics · FY 2025
- VAI
Foodborne Biological Hazards
Food/Cosmetics · FY 2025
Citation pattern
What the linked rows show
The dataset links 3 citation rows across 3 unique cited provisions. The leading references are 21 CFR 117.135(a), 21 CFR 117.190(a), and 21 CFR 117.80(c). Citation rows can reflect Form FDA 483 observations and are not necessarily citations in a final classification letter.
| Provision | Rows | Posted description |
|---|---|---|
| 21 CFR 117.135(a) | 1 | Sanitation preventive controls - Implement |
| 21 CFR 117.190(a) | 1 | Sanitation preventive controls - Implementation records |
| 21 CFR 117.80(c) | 1 | Manufacturing, processing, packing, holding - Controls |
Citations
CFR · FD&C Act
- 21 CFR 117.80(c)Read current eCFR
Manufacturing, processing, packing, holding - Controls
Foods
Title 21 · Part 117 · Sec 80Inspection has exact citation - 21 CFR 117.135(a)(1)Read current eCFR
Sanitation preventive controls - Implement
Foods
Title 21 · Part 117 · Sec 135Inspection has exact citation - 21 CFR 117.190(a)Read current eCFR
Sanitation preventive controls - Implementation records
Foods
Title 21 · Part 117 · Sec 190Inspection has exact citation
Form FDA 483 candidate audit
Every same-FEI index candidate · relationship confidence
For Taylor Farms Colorado, Inc. inspection 1253867, the audit considered 1 same-FEI Form 483 candidate: 1 high-confidence FEI/date link, 0 firm-context candidates, and 0 date-conflicting exclusions.
No Form FDA 483 or EIR document text has been reviewed in this local corpus. Citation rows and index metadata are not used to reconstruct investigator observations. Form FDA 483 observations are not a final FDA violation determination.
Primary-document observation evidence
Form FDA 483 or EIR text only
Taylor Farms Colorado, Inc. inspection 1253867 has no reviewed Form FDA 483 or EIR document text in the local corpus. No observation summary is generated from citation rows, index metadata, search snippets, or another inspection.
No observation summary is generated because no exact Form FDA 483 or EIR document text has been reviewed for this record.
Form FDA 483 observations are investigators’ observations and do not constitute a final FDA determination that a law or regulation was violated.
Taylor Farms Colorado, Inc. inspection history
Distinct inspection IDs · bounded historical context
The current public dataset links 6 distinct inspections to Taylor Farms Colorado, Inc., spanning October 8, 2008 through November 5, 2025. Relative to inspection 1253867, it contains 4 earlier and 1 later inspection. 0 cited provisions recur across at least two inspection IDs.
OAI inspections
0
Distinct inspection IDs containing at least one project-area row with this code.
VAI inspections
1
Distinct inspection IDs containing at least one project-area row with this code.
NAI inspections
5
Distinct inspection IDs containing at least one project-area row with this code.
UNKNOWN inspections
0
Distinct inspection IDs with no normalized final classification.
| Inspection | Ended | Classification | Project areas | Citations |
|---|---|---|---|---|
| 1290312 | Nov 05, 2025 | NAI | Foodborne Biological Hazards | 0 |
| 1253867This record | Nov 12, 2024 | VAI | Food Composition, Standards, Labeling and Econ, Foodborne Biological Hazards | 3 |
| 1130521 | Aug 31, 2020 | NAI | Foodborne Biological Hazards | 0 |
| 1022667 | Aug 02, 2017 | NAI | Foodborne Biological Hazards | 0 |
| 890942 | Aug 12, 2014 | NAI | Foodborne Biological Hazards | 0 |
| 542189 | Oct 08, 2008 | NAI | Food and Color Additives Petition Review, Foodborne Biological Hazards | 0 |
Provisions recurring across inspection IDs
No normalized provision appears in citation rows for at least two distinct inspection IDs in the current dataset. This is a bounded coverage result, not proof that no repeated observation existed.
- Counts reflect only inspections included in the current public FDA dataset; FDA states that the database is not comprehensive.
- Several project-area rows can share one inspection ID, so history counts are deduplicated by inspection ID.
- A repeated CFR provision is a recurrence in posted citation rows, not proof that the underlying facts, root causes, severity, or corrective-action effectiveness were the same.
- Changes from OAI to VAI or NAI, or the reverse, do not by themselves establish improvement or deterioration because scope, timing, evidence, and project areas can differ.
- Later public records are relevant historical context but still do not certify the facility’s current compliance or supplier suitability.
Regulatory follow-up
Independent source required
Taylor Farms Colorado, Inc. inspection 1253867 has no independently researched regulatory follow-up in this generated profile. Exact Warning Letter, import-alert, recall, injunction, seizure, and other enforcement sources remain unresearched.
Warning Letters, import alerts, recalls, injunctions, seizures, and other actions remain unresearched for this generated profile.
An inspection classification does not, by itself, establish that FDA issued a Warning Letter, import alert, recall, injunction, seizure, or any other specific follow-up action.
Evidence coverage
Present data · explicit gaps · review queue
| Source area | Status | What the status means |
|---|---|---|
| inspection classification | present | 2 exact classification rows join to InspectionID 1253867. |
| inspection citations | present | 3 citation rows join by exact InspectionID. |
| published 483 index | present | 1 same-FEI index candidate were evaluated and retained in the audit ledger. |
| form 483 document | not researched | No exact Form FDA 483 or EIR document text is stored or reviewed in the local inspection corpus, so no observation summary is generated. |
| firm history | present | Facility history is derived from exact FEI rows and deduplicated by InspectionID. |
| warning letters | not researched | Exact FDA Warning Letter sources have not been researched for this generated record. |
| import alerts | not researched | Exact FDA import-alert sources have not been researched for this generated record. |
| recalls | not researched | Exact FDA recall sources have not been researched for this generated record. |
| other enforcement | not researched | Other exact FDA enforcement sources have not been researched for this generated record. |
Human review pending. This deterministic profile has not received human regulatory review. Source gaps and candidate decisions remain visible for review.
How to use this record for due diligence
A five-step evidence workflow
- 1
Confirm identity, date, and inspected scope
Verify InspectionID 1253867, FEI 1783599, each project-area row, product type, location, and inspection end date against the FDA classification source. A classification applies to the closed inspected scope; it cannot be generalized to another site, product, project area, or current operating state.
- 2
Audit every Form 483 candidate
Review all 1 same-FEI index candidate, preserving FEI/date matches, firm-only context, and date conflicts rather than selecting a convenient record. The public index may omit InspectionID. FEI alone identifies facility context but does not prove that a document belongs to this exact inspection.
- 3
Read the actual inspection documents
Obtain and read the exact Form FDA 483 and EIR before summarizing observations; retain observation numbers, investigator examples, page locators, redactions, and document limitations. Citation rows and index metadata cannot reconstruct investigator observations, and a Form FDA 483 is not a final agency violation determination.
- 4
Map requirements to response and CAPA evidence
Use the exact citation rows and current eCFR navigation, then compare the primary observations with the firm response, root-cause analysis, corrective actions, preventive actions, and effectiveness evidence. A provision label alone does not disclose the observed facts, severity, root cause, remediation quality, or present operating controls.
- 5
Research subsequent records independently
Search later inspections, exact FDA Warning Letters, import alerts, recalls, and enforcement records, then obtain current facility evidence before making a material supplier decision. OAI does not identify a particular action, while any closed classification remains historical evidence rather than a current compliance or supplier verdict.
Sources, freshness, and limitations
Provenance you can audit
Official FDA sources
The newest source timestamp attached to this record is . FDA states that dashboard inspection and compliance data is refreshed weekly and remains subject to change.
Interpretive limits
- FDA classifies inspection project areas separately; one inspection ID can contain more than one outcome.
- A classification describes the closed inspection, not the establishment’s current compliance status or suitability as a supplier.
- A Form FDA 483 records investigators’ observations and is not a final agency determination that a law or regulation was violated.
- No linked citation or published 483 means no matching row was found in these sources; it does not prove no observation or Form 483 existed.
- The FDA inspection database is not comprehensive, includes closed inspections with final classifications, and is subject to change.
FDA inspection 1253867: questions answered
Record-specific FAQ
- What does FDA report for inspection 1253867?
- Taylor Farms Colorado, Inc. inspection 1253867 ended November 12, 2024. FDA posted VAI: Voluntary Action Indicated across 2 project-area rows, and the local corpus joins 3 exact citation rows. This is the closed inspection record, not a current facility verdict.
- What does VAI mean for inspection 1253867?
- Taylor Farms Colorado, Inc. inspection 1253867 has VAI: Voluntary Action Indicated. FDA found objectionable conditions or practices, but the agency was not prepared to take or recommend administrative or regulatory action. Voluntary correction is expected. If several project-area codes are posted, the headline is only a navigation summary; interpret every visible row within its inspected scope.
- Which provisions are linked to inspection 1253867?
- Taylor Farms Colorado, Inc. inspection 1253867 has 3 exact InspectionID citation rows grouped into 3 normalized provisions, led by 21 CFR 117.135(a), 21 CFR 117.190(a), and 21 CFR 117.80(c). Posted citation descriptions support requirement analysis but do not reproduce the investigator’s complete observations or a final classification letter.
- Is a Form FDA 483 linked to inspection 1253867?
- Taylor Farms Colorado, Inc. inspection 1253867 has 1 high-confidence Form 483 index link, 0 firm-context candidates, and 0 date-conflicting candidates. None is called an exact InspectionID match because the admitted OII index rows do not expose that identifier.
- What scope did inspection 1253867 cover?
- Taylor Farms Colorado, Inc. inspection 1253867 covers Food Composition, Standards, Labeling and Econ and Foodborne Biological Hazards for Food/Cosmetics at Colorado Springs, Colorado, United States. The page preserves every exact project-area row, classification, fiscal year, and additional detail; it does not generalize beyond that closed scope.
- What other FDA inspections are linked to this facility?
- Taylor Farms Colorado, Inc. inspection 1253867 belongs to an exact-FEI history containing 6 distinct inspection IDs, including 4 earlier and 1 later record relative to the target. Counts are deduplicated by InspectionID and remain historical context, not a compliance score.
- Do cited provisions recur across this facility’s inspections?
- Taylor Farms Colorado, Inc. inspection 1253867 is in a current facility history where no normalized provision appears across at least two distinct InspectionIDs. This bounded corpus result does not prove that no observation recurred because inspection, citation, and document coverage may be incomplete or unavailable.
- Did FDA take action after inspection 1253867?
- Taylor Farms Colorado, Inc. inspection 1253867 has no independently researched follow-up action in this generated profile. Warning Letters, import alerts, recalls, injunctions, seizures, and other actions remain explicitly unresearched; VAI alone cannot establish that any particular action occurred or describe the firm’s response.
- Does inspection 1253867 establish current compliance?
- Taylor Farms Colorado, Inc. inspection 1253867 does not establish the facility’s current compliance, supplier suitability, future performance, or remediation success. VAI describes FDA’s final classification of a closed inspection and its posted project-area scope. Current decisions require later official records plus current quality-system, CAPA, and operational evidence.
- How complete is the record for inspection 1253867?
- Taylor Farms Colorado, Inc. inspection 1253867 includes exact classification rows, 3 exact citation rows, and a complete same-FEI Form 483 candidate audit for the loaded corpus. It does not include reviewed Form 483 or EIR text or independently researched enforcement sources, and FDA says its inspection database is not comprehensive.
- How should inspection 1253867 be used in due diligence?
- Use Taylor Farms Colorado, Inc. inspection 1253867 to anchor identity, date, scope, classifications, exact citations, candidate documents, and facility history. Then read the primary inspection documents, map observations to requirements and CAPA evidence, research subsequent FDA actions separately, and obtain current evidence before making a supplier or compliance decision.
Built from FDA final-classification and citation rows plus the OII FOIA Electronic Reading Room. Citation rows join by FDA Inspection ID; published Form 483 records are linked conservatively by FEI and, when available, matching record and inspection dates. Relationship evidence is disclosed rather than presented as certainty.
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