FDA Inspection
TriRx Huntsville Pharmaceutical Services, LLCTriRx Huntsville Pharmaceutical Services, LLC – FDA Inspection, Jun 15, 2026
Record Details
This FDA Inspection record concerns TriRx Huntsville Pharmaceutical Services, LLC, with an inspection on June 15, 2026, issued by the New Orleans District Office, covering human drugs.
- Inspection Date
- June 15, 2026
- Product Type
- Human Drugs
View Company Profile
ID · 84548e82-46e0-4e70-b7ac-63ce50cfbc7f
Inspection Facts
- Inspection number
- 1322326
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
5- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.165(e)Test methods
- 21 CFR 211.198(a)Adverse Drug Experience
- 21 CFR 211.67(b)Written procedures not established/followed
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
Full citation text and observation details available on the Dashboard.
Other FDA inspections of TriRx Huntsville Pharmaceutical Services, LLC
13| Date | Classification | Office | Project area |
|---|---|---|---|
| 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 |
| August 1, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for TriRx Huntsville Pharmaceutical Services, LLC
- FDA Inspection 1216782 - 2023-08-11
- FDA Inspection 1166895 - 2022-04-01
- FDA Inspection 978625 - 2016-04-21
- FDA Inspection 908381 - 2014-12-19
- FDA Inspection 891076 - 2014-08-01
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