FDA Inspection
Oxid CorporationOxid Corporation – FDA Inspection, May 23, 2024
Record Details
This FDA Inspection record concerns Oxid Corporation, with an inspection on May 23, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 8714e814-a7d7-465c-ab08-28496ede1706
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1239248
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.72(b)Calibration procedures - content
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