FDA Inspection 1195162 — Midwest Sterilization Corporation

Midwest Sterilization Corporation — FEI 3005012805

The FDA completed an inspection of Midwest Sterilization Corporation on Jan 12, 2023 in Laredo, TX. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jan 12, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Laredo, TX (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

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