# AstraZeneca Dunkerque Production (AZDP) - Inspection Records

Source: https://www.globalkeysolutions.net/companies/astrazeneca-dunkerque-production-azdp/581c1e69-c574-45d9-a5e0-a263fc2e4c6c

> Inspection records and compliance data for AstraZeneca Dunkerque Production (AZDP) in Dordogne, None. Access full analysis and detailed observations.

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## Details

- Name: AstraZeneca Dunkerque Production (AZDP)
- FEI Number: 3003063819
- City: Dordogne
- State: None
- Country Name: France
- Address Line 1: Zone Entree Noord Gracht, 224 Avenue De La Dordogne
- Zip Code: None

## Related Documents

- [FDA Inspection 1275115 - AstraZeneca Dunkerque Production (AZDP) - 2022-02-03](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/64c14df4-1cf0-40cf-8ed3-2d05ef102946) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 3, 2022
- [FDA Inspection 1101056 - AstraZeneca Dunkerque Production (AZDP) - 2018-12-21](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/5004d23f-0fc7-4869-8ebe-a9d635c4e8b0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2018
- [FDA Inspection 961861 - AstraZeneca Dunkerque Production (AZDP) - 2015-11-20](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/5d2047f6-4703-4457-aa42-7c3cfd6b85fa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2015
- [FDA Inspection 839238 - AstraZeneca Dunkerque Production (AZDP) - 2013-05-17](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/223edaed-d0d3-4f3e-9d29-12dcc46404a7) — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2013
- [FDA Inspection 560743 - AstraZeneca Dunkerque Production (AZDP) - 2009-01-30](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/29884e1f-03d5-425b-9f1a-a3bd20d3a1a4) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2009

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