# FDA Inspection 734695 - Sanofi S.r.l. - June 23, 2011

Source: https://www.keypedia.com/records/fda_inspections/sanofi-srl/2edb15ce-bd0d-4f67-96ad-3b6a5f974895
Source feed: FDA_Inspections

> FDA Inspection 734695 for Sanofi S.r.l. on June 23, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 734695
- Company Name: Sanofi S.r.l.
- Inspection Date: 2011-06-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234890 - 2024-06-21](https://www.keypedia.com/records/fda_inspections/sanofi-srl/28e62a0d-2109-4427-9fe0-c6ec583b5df3)
- [FDA Inspection 1205901 - 2021-11-18](https://www.keypedia.com/records/fda_inspections/sanofi-srl/045c53c0-cc89-4d23-9620-cfeabf5f2815)
- [FDA Inspection 1123330 - 2019-02-15](https://www.keypedia.com/records/fda_inspections/sanofi-srl/3c8c9988-0e18-4f9d-b56d-8108fd6f5333)
- [FDA Inspection 1055081 - 2018-05-31](https://www.keypedia.com/records/fda_inspections/sanofi-srl/f2051720-276f-4ae9-ae91-53a9ea4332d2)
- [FDA Inspection 988968 - 2016-07-29](https://www.keypedia.com/records/fda_inspections/sanofi-srl/58bbc22a-ca71-40a7-a372-9df31c203e5b)

Company: https://www.keypedia.com/companies/sanofi-srl/54ba861a-36eb-4486-a4ba-2a8194cdf7a5

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