FDA Warning Letter — Hooper Holmes, Inc.

Case 138390 — FEI 1000118383

The FDA took a Warning Letter action against Hooper Holmes, Inc. on December 22, 2010 (Olathe, KS). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Hooper Holmes, Inc.
Date
December 22, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Olathe, KS (United States)