FDA Inspection 1151308 — Midwest Sterilization Corporation

Midwest Sterilization Corporation — FEI 1928237

The FDA completed an inspection of Midwest Sterilization Corporation on September 2, 2021 in Jackson, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 2, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Jackson, MO (United States)

Additional Details

Postmarket Audit Inspections