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FDA Inspection 1071153 — Midwest Sterilization Corporation

Midwest Sterilization Corporation — FEI 1928237

The FDA completed an inspection of Midwest Sterilization Corporation on November 7, 2018 in Jackson, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 7, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Jackson, MO (United States)

Facility

Other inspections at this facility

  • 1230329 (VAI Fri Feb 16 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1190354 (OAI Thu Nov 10 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1151308 (OAI Thu Sep 02 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1045726 (VAI Thu Mar 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 931438 (VAI Thu Jun 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources