FDA Inspection
Teva Parenteral Medicines, Inc.Teva Parenteral Medicines, Inc. – FDA Inspection, Apr 24, 2012
Record Details
This FDA Inspection record concerns Teva Parenteral Medicines, Inc., with an inspection on April 24, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- April 24, 2012
- Product Type
- Drugs
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ID · cbf10a34-d00d-4548-bb82-13db30750338
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 779321
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.42(c)(10)(iv)Environmental Monitoring System
- 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
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Other FDA inspections of Teva Parenteral Medicines, Inc.
11| Date | Classification | Office | Project area |
|---|---|---|---|
| August 20, 2021 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 30, 2019 | NAI | Center for Drug Evaluation and Research | New Drug Evaluation |
| January 18, 2019 | VAI | Los Angeles District Office | Generic Drug Evaluation |
| December 19, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 29, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Teva Parenteral Medicines, Inc.
- FDA Inspection 1149378 - 2021-08-20
- FDA Inspection 1100853 - 2019-08-30
- FDA Inspection 1077528 - 2019-01-18
- FDA Inspection 997582 - 2016-12-19
- FDA Inspection 980903 - 2016-07-29
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