FDA Inspection 1239248 — Oxid Corporation

Oxid Corporation — FEI 3017929928

The FDA completed an inspection of Oxid Corporation on May 23, 2024 in Novi, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Novi, MI (United States)

Citations

IDCFRDescription
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures
323621 CFR 820.72(b)Calibration procedures - content
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures