FDA Warning Letter — Herman A. Jenkins, MD

Case 120908 — FEI 3008351459

The FDA took a Warning Letter action against Herman A. Jenkins, MD on August 16, 2010 (Aurora, CO). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Herman A. Jenkins, MD
Date
August 16, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Aurora, CO (United States)