# FDA Inspection 590027 - Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC - June 04, 2009

Source: https://www.keypedia.com/records/fda_inspections/wyeth-biopharma-division-of-wyeth-pharmaceuticals-llc/9876ffaf-133a-4fbe-8af5-86ed840c725c
Source feed: FDA_Inspections

> FDA Inspection 590027 for Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC on June 04, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 590027
- Company Name: Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC
- Inspection Date: 2009-06-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/wyeth-biopharma-division-of-wyeth-pharmaceuticals-llc/0de9118f-18ec-45b8-b757-44f97c13c29c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7