FDA Inspection 885787 — Precept Medical Products Inc

Precept Medical Products Inc — FEI 2017510

The FDA completed an inspection of Precept Medical Products Inc on Jun 20, 2014 in Douglas, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 20, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Douglas, AZ (United States)