FDA Warning Letter — Radnostix

Case 215994 — FEI 3003350319

The FDA took a Warning Letter action against Radnostix on October 26, 2011 (Idaho Falls, ID). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Radnostix
Date
October 26, 2011
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Idaho Falls, ID (United States)