FDA Inspection 1108577 — Centurion Medical Products, LP

Centurion Medical Products, LP — FEI 3008403546

The FDA completed an inspection of Centurion Medical Products, LP on November 1, 2019 in Williamston, MI. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 1, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Williamston, MI (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
310421 CFR 820.30(j)Design history file
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation