FDA Warning Letter — PhotoMedex, Inc.

Case 225674 — FEI 3000206133

The FDA took a Warning Letter action against PhotoMedex, Inc. on Jan 26, 2012 (Horsham, PA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
PhotoMedex, Inc.
Date
Jan 26, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Horsham, PA (United States)