FDA Inspection 908610 — Procedure Products, Inc.

Procedure Products, Inc. — FEI 3020778

The FDA completed an inspection of Procedure Products, Inc. on Jan 5, 2015 in Vancouver, WA. 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
Jan 5, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Vancouver, WA (United States)