FDA Inspection
TriRx Huntsville Pharmaceutical Services, LLCTriRx Huntsville Pharmaceutical Services, LLC – FDA Inspection, Apr 14, 2011
Record Details
This FDA Inspection record concerns TriRx Huntsville Pharmaceutical Services, LLC, with an inspection on April 14, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- April 14, 2011
- Product Type
- Drugs
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ID · 341020b5-3b59-4356-a9d3-1a53a4e6a79f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 721339
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.192Extent of discrepancy, failure investigations
- 21 CFR 211.80(a)Written Procedures Not Followed
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Other FDA inspections of TriRx Huntsville Pharmaceutical Services, LLC
13| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2026 | Not classified | New Orleans District Office | Drug Quality Assurance |
| August 11, 2023 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 1, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 21, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 19, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for TriRx Huntsville Pharmaceutical Services, LLC
- FDA Inspection 1322326 - 2026-06-15
- FDA Inspection 1216782 - 2023-08-11
- FDA Inspection 1166895 - 2022-04-01
- FDA Inspection 978625 - 2016-04-21
- FDA Inspection 908381 - 2014-12-19
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