FDA Inspection 1205081 - D. O. Weaver and Company - May 12, 2023

Record Details

This FDA Inspection record concerns D. O. Weaver and Company, with an inspection on May 12, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: D. O. Weaver and Company
Inspection Date: May 12, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 2d9a3a09-8d9d-4cf4-9a42-a62dffb9b9a4

Violation Codes2

21 CFR 820.198(d)21 CFR 820.75(a)

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