FDA Inspection 1190354 — Midwest Sterilization Corporation

Midwest Sterilization Corporation — FEI 1928237

The FDA completed an inspection of Midwest Sterilization Corporation on November 10, 2022 in Jackson, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 10, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Jackson, MO (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ