# 3M Espe Dental Products – FDA Inspection, Jan 27, 2010

Source: https://www.keypedia.com/records/fda_inspections/3m-espe-dental-products/ede323f0-8bb1-4b05-8095-ce824a2ceb6b
Source feed: FDA_Inspections

> FDA inspection 641481 of 3M Espe Dental Products, January 27, 2010. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 641481
- Company Name: 3M Espe Dental Products
- Inspection Date: 2010-01-27
- 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 910135 - 2015-01-15](https://www.keypedia.com/records/fda_inspections/3m-espe-dental-products/2ef9261b-563c-4a62-8162-d0378d0b16a9)
- FDA Inspection 802882 - 2012-10-05

Company: https://www.keypedia.com/companies/3m-espe-dental-products/9aded764-aced-4527-9616-b1fc9e9307c4

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