FDA Inspection 1197992 — NAMSA

NAMSA — FEI 3004109681

The FDA completed an inspection of NAMSA on Feb 8, 2023 in Minneapolis, MN. 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
Feb 8, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

Sponsor, Contract Research Organization