FDA Inspection
D. O. Weaver and CompanyD. O. Weaver and Company – FDA Inspection, Nov 10, 2016
Record Details
This FDA Inspection record concerns D. O. Weaver and Company, with an inspection on November 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · bbcfbd7d-16ea-40f9-a0eb-6f81744c601f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 995563
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.75(a)Lack of or inadequate process validation
Full citation text and observation details available on the Dashboard.
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 |
| October 13, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for D. O. Weaver and Company
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.