FDA Warning Letter — Hiossen Inc.

Case 315338 — FEI 3007135442

The FDA took a Warning Letter action against Hiossen Inc. on October 5, 2012 (Fairless Hills, PA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Hiossen Inc.
Date
October 5, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Fairless Hills, PA (United States)