FDA Inspection 983441 — OsteoCentric Technologies, Inc.

OsteoCentric Technologies, Inc. — FEI 3011656326

The FDA completed an inspection of OsteoCentric Technologies, Inc. on Aug 30, 2016 in Logan, UT. 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
Aug 30, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Logan, UT (United States)