# FDA Inspection 1031032 - Wyeth Pharmaceuticals Llc - August 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/wyeth-pharmaceuticals-llc/f5dd2b5f-3635-4d4e-94d7-24b42ec867f5
Source feed: FDA_Inspections

> FDA Inspection 1031032 for Wyeth Pharmaceuticals Llc on August 29, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031032
- Company Name: Wyeth Pharmaceuticals Llc
- Inspection Date: 2017-08-29
- 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 844357 - 2013-08-15](https://www.keypedia.com/records/fda_inspections/wyeth-pharmaceuticals-llc/970c33bb-c906-4ced-8cc3-026a464f33f0)
- [FDA Inspection 834523 - 2013-06-06](https://www.keypedia.com/records/fda_inspections/wyeth-pharmaceuticals-llc/cb0eda6f-7ce2-401f-9e92-cc3bbc286267)
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Company: https://www.keypedia.com/companies/wyeth-pharmaceuticals-llc/351451d6-3ff5-4bc3-b1d5-9cefe38d7c3c

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