FDA Warning Letter — Gentell, Inc

Case 479251 — FEI 1000522686

The FDA took a Warning Letter action against Gentell, Inc on October 5, 2015 (Bristol, PA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Gentell, Inc
Date
October 5, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Bristol, PA (United States)