FDA Inspection 1064644 — Primus Corporation

Primus Corporation — FEI 1931251

The FDA completed an inspection of Primus Corporation on September 6, 2018 in Kansas City, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 6, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Kansas City, MO (United States)

Citations

IDCFRDescription
316021 CFR 820.184Lack of or inadequate DHR procedures