# D. O. Weaver and Company – FDA Inspection, May 12, 2023

Source: https://www.keypedia.com/records/fda_inspections/d-o-weaver-and-company/f63ae782-4c99-470f-a51f-46c05d5f7a2d
Source feed: FDA_Inspections

> FDA inspection 1205081 of D. O. Weaver and Company, May 12, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205081
- Company Name: D. O. Weaver and Company
- Inspection Date: 2023-05-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 995563 - 2016-11-10](https://www.keypedia.com/records/fda_inspections/d-o-weaver-and-company/bbcfbd7d-16ea-40f9-a0eb-6f81744c601f)
- [FDA Inspection 625093 - 2009-10-13](https://www.keypedia.com/records/fda_inspections/d-o-weaver-and-company/736f7d6a-6e3a-4941-8efd-edeb2573a089)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

Company: https://www.keypedia.com/companies/d-o-weaver-and-company/9d3abd0b-5acb-4fea-800f-ff8cb0a9daeb

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7