FDA Warning Letter — Oscor Inc.

Case 496385 — FEI 1035166

The FDA took a Warning Letter action against Oscor Inc. on June 13, 2016 (Palm Harbor, FL). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Oscor Inc.
Date
June 13, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Palm Harbor, FL (United States)