FDA Inspection 825245 — Midwest Sterilization Corporation

Midwest Sterilization Corporation — FEI 3005012805

The FDA completed an inspection of Midwest Sterilization Corporation on Mar 28, 2013 in Laredo, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 28, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Laredo, TX (United States)

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