FDA Inspection
Midwest Sterilization CorporationMidwest Sterilization Corporation – FDA Inspection, Jun 18, 2015
Record Details
This FDA Inspection record concerns Midwest Sterilization Corporation, with an inspection on June 18, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 18, 2015
- Product Type
- Devices
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ID · 97d35b69-599a-4d40-9f14-59d92b25cf38
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 931438
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
- 21 CFR 820.50(a)(2)Supplier oversight
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Other FDA inspections of Midwest Sterilization Corporation
8| Date | Classification | Office | Project area |
|---|---|---|---|
| July 16, 2026 | Not classified | Kansas City District Office | Project Evaluation: Devices |
| February 16, 2024 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 10, 2022 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 2, 2021 | OAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| November 7, 2018 | VAI | Center for Devices and Radiological Health | Project Evaluation: Devices |
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