# FDA Inspection 813433 - 3M COMPANY - December 05, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/3m-company/4248a044-093d-4b14-bff8-7edc18c0e25c
Source feed: FDA_Inspections

> FDA Inspection 813433 for 3M COMPANY on December 05, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 813433
- Company Name: 3M COMPANY
- Inspection Date: 2012-12-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1060963 - 2018-05-25](https://www.globalkeysolutions.net/records/fda_inspections/3m-company/cb4c3411-7dfc-4560-83cc-1b8f44c96633)
- [FDA Inspection 813433 - 2012-12-05](https://www.globalkeysolutions.net/records/fda_inspections/3m-company/28616565-49c0-45c0-82f2-5719e6773eaa)
- [FDA Inspection 660586 - 2010-04-27](https://www.globalkeysolutions.net/records/fda_inspections/3m-company/daf778c1-a16a-4242-bc38-980183a5b8e6)

Company: https://www.globalkeysolutions.net/companies/3m-company/999d0f59-ffb0-48ec-8825-7d5ce4070dc3

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