FDA Inspection 1154127 — Promega Corporation

Promega Corporation — FEI 3002622561

The FDA completed an inspection of Promega Corporation on August 25, 2021 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
August 25, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fitchburg, WI (United States)

Additional Details

Postmarket Audit Inspections