FDA Inspection 1045726 — Midwest Sterilization Corporation

Midwest Sterilization Corporation — FEI 1928237

The FDA completed an inspection of Midwest Sterilization Corporation on Mar 22, 2018 in Jackson, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 22, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Jackson, MO (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.