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FDA Inspection
•Midwest Sterilization Corporation•September 2, 2021

Midwest Sterilization Corporation – FDA Inspection, Sep 2, 2021

Record Details

This FDA Inspection record concerns Midwest Sterilization Corporation, with an inspection on September 2, 2021, issued by the Center for Devices and Radiological Health, covering devices.

Company
Midwest Sterilization Corporation
Inspection Date
September 2, 2021
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · af38af1b-66c0-4019-a177-addbc148fc1a

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1151308
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

Other FDA inspections of Midwest Sterilization Corporation

8
DateClassificationOfficeProject area
July 16, 2026Not classifiedKansas City District OfficeProject Evaluation: Devices
February 16, 2024VAICenter for Devices and Radiological HealthCompliance: Devices
November 10, 2022OAICenter for Devices and Radiological HealthCompliance: Devices
November 7, 2018VAICenter for Devices and Radiological HealthProject Evaluation: Devices
March 22, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
View all 8 other inspections on the company page
Other documents for Midwest Sterilization Corporation
  • FDA Inspection 1326636 - 2026-07-16
  • FDA Inspection 1230329 - 2024-02-16
  • FDA Inspection 1190354 - 2022-11-10
  • FDA Inspection 1071153 - 2018-11-07
  • FDA Inspection 1045726 - 2018-03-22

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Contact
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