FDA Warning Letter — Gunnell Llc

Case 131691 — FEI 3009255757

The FDA took a Warning Letter action against Gunnell Llc on November 9, 2010 (Elk City, OK). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Gunnell Llc
Date
November 9, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Elk City, OK (United States)