FDA Warning Letter — James P. Johnston, CO

Case 82424 — FEI 1823996

The FDA took a Warning Letter action against James P. Johnston, CO on Mar 17, 2010 (Michigan City, IN). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
James P. Johnston, CO
Date
Mar 17, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Michigan City, IN (United States)