FDA Inspection 802882 — 3M Espe Dental Products

3M Espe Dental Products — FEI 2020493

The FDA completed an inspection of 3M Espe Dental Products on Oct 5, 2012 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 5, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.