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FDA Inspection 819082 — Midwest Sterilization Corporation

Midwest Sterilization Corporation — FEI 1928237

The FDA completed an inspection of Midwest Sterilization Corporation on February 12, 2013 in Jackson, MO. 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
February 12, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Jackson, MO (United States)

Facility

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