FDA Inspection 1266843 — 3M Company IRB

3M Company IRB — FEI 3009666037

The FDA completed an inspection of 3M Company IRB on April 7, 2025 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 7, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Saint Paul, MN (United States)

Additional Details

IRB