FDA Warning Letter — Thomas K Jones MD - Clinical Investigator

Case 56623 — FEI 3007455800

The FDA took a Warning Letter action against Thomas K Jones MD - Clinical Investigator on Jul 1, 2009 (Seattle, WA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Thomas K Jones MD - Clinical Investigator
Date
Jul 1, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Seattle, WA (United States)