FDA Warning Letter — Electro Medical, Inc.

Case 407188 — FEI 1000117937

The FDA took a Warning Letter action against Electro Medical, Inc. on August 9, 2013 (Tulsa, OK). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Electro Medical, Inc.
Date
August 9, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Tulsa, OK (United States)