# 3M Espe Dental Products - Inspection Records

Source: https://www.globalkeysolutions.net/companies/3m-espe-dental-products/af4cf703-2a63-443e-8983-6ae31d09b94c

> Inspection records and compliance data for 3M Espe Dental Products in Saint Paul, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: 3M Espe Dental Products
- FEI Number: 3005174370
- City: Saint Paul
- State: Minnesota
- Country Name: United States
- Address Line 1: 2510 Conway Ave E Bldg 260-02a-11
- Zip Code: 55144

## Related Documents

- [FDA Inspection 1046452 - 3M Espe Dental Products - 2018-03-07](https://www.globalkeysolutions.net/records/fda_inspections/3m-espe-dental-products/dd63e526-27a1-4a8a-ad3f-a5f040b17a63) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2018
- [FDA Inspection 872250 - 3M Espe Dental Products - 2014-03-12](https://www.globalkeysolutions.net/records/fda_inspections/3m-espe-dental-products/daf40ede-3ef0-439a-af0e-a6e89827bca6) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2014
- [FDA Inspection 799456 - 3M Espe Dental Products - 2012-09-20](https://www.globalkeysolutions.net/records/fda_inspections/3m-espe-dental-products/4da19b3e-eeb0-4356-a9a7-36355ace144a) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2012
- [FDA Inspection 799456 - 3M Espe Dental Products - 2012-09-20](https://www.globalkeysolutions.net/records/fda_inspections/3m-espe-dental-products/9a8ce6fd-9cba-408d-bf9b-ae15800a96d9) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2012
- [FDA Inspection 698056 - 3M Espe Dental Products - 2010-11-19](https://www.globalkeysolutions.net/records/fda_inspections/3m-espe-dental-products/80e6bb3a-b5ed-4721-96a6-6bbb65f4ed22) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 19, 2010
- [FDA Inspection 579363 - 3M Espe Dental Products - 2009-03-13](https://www.globalkeysolutions.net/records/fda_inspections/3m-espe-dental-products/7118c5d6-dd0c-476b-9843-545ad5a31b4c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 13, 2009

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