FDA Inspection 1253535 — Promega Corporation

Promega Corporation — FEI 3002622561

The FDA completed an inspection of Promega Corporation on October 29, 2024 in Fitchburg, WI. 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
October 29, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fitchburg, WI (United States)

Additional Details

Sponsor, Contract Research Organization