# FDA Inspection 649019 - 3M Deutschland GmbH - January 28, 2010

Source: https://www.keypedia.com/records/fda_inspections/3m-deutschland-gmbh/f09ab671-6977-480d-ae59-a710b9612895
Source feed: FDA_Inspections

> FDA Inspection 649019 for 3M Deutschland GmbH on January 28, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 649019
- Company Name: 3M Deutschland GmbH
- Inspection Date: 2010-01-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/3m-deutschland-gmbh/db35276e-cd82-48aa-b806-7dc4748d262b

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