FDA Inspection 965801 — Allpro, Inc.

Allpro, Inc. — FEI 1000117439

The FDA completed an inspection of Allpro, Inc. on April 5, 2016 in Broomfield, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 5, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Broomfield, CO (United States)