FDA Inspection
D. O. Weaver and CompanyD. O. Weaver and Company – FDA Inspection, Oct 13, 2009
Record Details
This FDA Inspection record concerns D. O. Weaver and Company, with an inspection on October 13, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- D. O. Weaver and Company
- Inspection Date
- October 13, 2009
- Product Type
- Devices
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ID · 736f7d6a-6e3a-4941-8efd-edeb2573a089
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 625093
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.75(a)Lack of or inadequate process validation
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Other FDA inspections of D. O. Weaver and Company
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 10, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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