# FDA Inspection 910135 - 3M Espe Dental Products - January 15, 2015

Source: https://www.keypedia.com/records/fda_inspections/3m-espe-dental-products/2ef9261b-563c-4a62-8162-d0378d0b16a9
Source feed: FDA_Inspections

> FDA Inspection 910135 for 3M Espe Dental Products on January 15, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 910135
- Company Name: 3M Espe Dental Products
- Inspection Date: 2015-01-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 802882 - 2012-10-05](https://www.keypedia.com/records/fda_inspections/3m-espe-dental-products/5c38b4e3-f4a5-4002-a8d2-be105aea9b65)
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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