# 3M Company – FDA Inspection, Sep 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/3m-company/32ee3c74-5887-4fce-8f21-af9274d6bf97
Source feed: FDA_Inspections

> FDA inspection 985519 of 3M Company, September 14, 2016. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 985519
- Company Name: 3M Company
- Inspection Date: 2016-09-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1135496 - 2019-06-21](https://www.keypedia.com/records/fda_inspections/3m-company/767273c8-4fe3-46ef-ae15-8f3e7aa7db38)
- FDA Inspection 858430 - 2013-12-13
- [FDA Inspection 709279 - 2011-02-11](https://www.keypedia.com/records/fda_inspections/3m-company/b2dac7af-c0b0-4a6c-9431-ed69550ff96a)

Company: https://www.keypedia.com/companies/3m-company/2c80adbb-d3a6-45c0-815c-4285addf5606

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