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FDA Inspection
•Midwest Sterilization Corporation•July 16, 2026

Midwest Sterilization Corporation – FDA Inspection, Jul 16, 2026

Record Details

This FDA Inspection record concerns Midwest Sterilization Corporation, with an inspection on July 16, 2026, issued by the Kansas City District Office, covering medical devices & rad health.

Company
Midwest Sterilization Corporation
Inspection Date
July 16, 2026
Product Type
Medical Devices & Rad Health
Office
Kansas City District Office
Person
  • Edward E. Lockwood (Issuing Officer)
View Company Profile

ID · 981274ae-761a-4c3b-aa86-e70bba9f441c

Inspection Facts

Inspection number
1326636
FDA center
Medical Devices & Rad Health
Project area
Project Evaluation: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. ISO 13485:2016 Clause 4.1.5Control over outsourced processes not proportionate to risk

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Midwest Sterilization Corporation

8
DateClassificationOfficeProject area
February 16, 2024VAICenter for Devices and Radiological HealthCompliance: Devices
November 10, 2022OAICenter 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 1230329 - 2024-02-16
  • FDA Inspection 1190354 - 2022-11-10
  • FDA Inspection 1151308 - 2021-09-02
  • FDA Inspection 1071153 - 2018-11-07
  • FDA Inspection 1045726 - 2018-03-22

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