# FDA Inspection 839238 - AstraZeneca Dunkerque Production (AZDP) - May 17, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/223edaed-d0d3-4f3e-9d29-12dcc46404a7
Source feed: FDA_Inspections

> FDA Inspection 839238 for AstraZeneca Dunkerque Production (AZDP) on May 17, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 839238
- Company Name: AstraZeneca Dunkerque Production (AZDP)
- Inspection Date: 2013-05-17
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1275115 - 2022-02-03](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/64c14df4-1cf0-40cf-8ed3-2d05ef102946)
- [FDA Inspection 1101056 - 2018-12-21](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/5004d23f-0fc7-4869-8ebe-a9d635c4e8b0)
- [FDA Inspection 961861 - 2015-11-20](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/5d2047f6-4703-4457-aa42-7c3cfd6b85fa)
- [FDA Inspection 560743 - 2009-01-30](https://www.globalkeysolutions.net/records/fda_inspections/astrazeneca-dunkerque-production-azdp/29884e1f-03d5-425b-9f1a-a3bd20d3a1a4)

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

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
