FDA Inspection
AstraZeneca Pharmaceuticals LPAstraZeneca Pharmaceuticals LP – FDA Inspection, Mar 20, 2013
Record Details
This FDA Inspection record concerns AstraZeneca Pharmaceuticals LP, with an inspection on March 20, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- March 20, 2013
- Product Type
- Drugs
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ID · ebf67d79-14af-41ab-a946-c03f62c78638
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 823366
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 314.80(c)(1)(i)Late submission of 15-day report
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Other FDA inspections of AstraZeneca Pharmaceuticals LP
15| Date | Classification | Office | Project area |
|---|---|---|---|
| January 14, 2026 | Not classified | Baltimore District Office | |
| October 25, 2024 | Not classified | Baltimore District Office | |
| May 31, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2024 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| July 18, 2023 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for AstraZeneca Pharmaceuticals LP
- FDA Inspection 1299436 - 2026-01-14
- FDA Inspection 1254239 - 2024-10-25
- FDA Inspection 1238346 - 2024-05-31
- FDA Inspection 1230136 - 2024-01-22
- FDA Inspection 1211604 - 2023-07-18
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