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FDA Inspection
•Midwest Sterilization Corporation•November 10, 2022

Midwest Sterilization Corporation – FDA Inspection, Nov 10, 2022

Record Details

This FDA Inspection record concerns Midwest Sterilization Corporation, with an inspection on November 10, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company
Midwest Sterilization Corporation
Inspection Date
November 10, 2022
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 30a00f53-abfd-4b16-a372-805941c0822a

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1190354
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 820.100(a)Lack of or inadequate procedures
  2. 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ

Full citation text and observation details available on the Dashboard.

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
September 2, 2021OAICenter for Devices and Radiological HealthBioresearch Monitoring
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 1151308 - 2021-09-02
  • FDA Inspection 1071153 - 2018-11-07
  • FDA Inspection 1045726 - 2018-03-22

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Contact
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370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
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Scranton, PA, 18503
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