FDA Inspection 944939 — Centurion Medical Products, LP

Centurion Medical Products, LP — FEI 1824619

The FDA completed an inspection of Centurion Medical Products, LP on September 21, 2015 in Howell, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 21, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Howell, MI (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures