FDA Warning Letter — Hiossen Inc.

Case 315338 — FEI 3007135442

The FDA took a Warning Letter action against Hiossen Inc. on Oct 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
Oct 5, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Fairless Hills, PA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.