FDA Inspection
AstraZeneca Dunkerque Production (AZDP)AstraZeneca Dunkerque Production (AZDP) – FDA Inspection, Nov 20, 2015
Record Details
This FDA Inspection record concerns AstraZeneca Dunkerque Production (AZDP), with an inspection on November 20, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- November 20, 2015
- Product Type
- Drugs
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ID · 5d2047f6-4703-4457-aa42-7c3cfd6b85fa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 961861
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of AstraZeneca Dunkerque Production (AZDP)
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 3, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 21, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 17, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 30, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for AstraZeneca Dunkerque Production (AZDP)
- FDA Inspection 1275115 - 2022-02-03
- FDA Inspection 1101056 - 2018-12-21
- FDA Inspection 839238 - 2013-05-17
- FDA Inspection 560743 - 2009-01-30
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