FDA Inspection
Actavis Laboratories UT, Inc.Actavis Laboratories UT, Inc. – FDA Inspection, Jan 14, 2011
Record Details
This FDA Inspection record concerns Actavis Laboratories UT, Inc., with an inspection on January 14, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- January 14, 2011
- Product Type
- Drugs
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ID · ae45d156-be5a-4379-8a0c-0ba4238d7b15
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 706470
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.192Extent of discrepancy, failure investigations
- 21 CFR 211.194(a)(8)Second person sign off
- 21 CFR 211.188(a)Accurate reproduction
- 21 CFR 211.100(b)SOPs not followed / documented
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Other FDA inspections of Actavis Laboratories UT, Inc.
12| Date | Classification | Office | Project area |
|---|---|---|---|
| September 19, 2025 | VAI | Denver District Office | Drug Quality Assurance |
| March 19, 2024 | OAI | Drug Quality Assurance | |
| August 20, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 2, 2018 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| October 25, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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- FDA Inspection 1035181 - 2017-10-25
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