# FDA Inspection 608890 - Sanofi US Services, Inc. - September 03, 2009

Source: https://www.keypedia.com/records/fda_inspections/sanofi-us-services-inc/d38f98c4-c4d9-4aa4-a2cf-8a8bc3b81dce
Source feed: FDA_Inspections

> FDA Inspection 608890 for Sanofi US Services, Inc. on September 03, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 608890
- Company Name: Sanofi US Services, Inc.
- Inspection Date: 2009-09-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/sanofi-us-services-inc/f353cbc0-ab3f-4c16-86a1-b9ee2af4e4a1

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