# 3M COMPANY – FDA Inspection, Dec 5, 2012

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

> FDA inspection 813433 of 3M COMPANY, December 05, 2012. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 813433
- Company Name: 3M COMPANY
- Inspection Date: 2012-12-05
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1060963 - 2018-05-25](https://www.keypedia.com/records/fda_inspections/3m-company/cb4c3411-7dfc-4560-83cc-1b8f44c96633)
- [FDA Inspection 1039481 - 2017-06-08](https://www.keypedia.com/records/fda_inspections/3m-company/8fa9809e-3ab4-4b85-9ecb-5f4b7b2e5259)
- FDA Inspection 660586 - 2010-04-27

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

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