FDA Inspection 1077604 — Oricare Inc.

Oricare Inc. — FEI 3009129579

The FDA completed an inspection of Oricare Inc. on December 11, 2018 in Quakertown, PA. 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
December 11, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Quakertown, PA (United States)