FDA Warning Letter — Richard K. Burt

Case 508253 — FEI 3012410440

The FDA took a Warning Letter action against Richard K. Burt on November 15, 2016 (Chicago, IL). The action was issued by CBER and concerns biologics products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Richard K. Burt
Date
November 15, 2016
Fiscal Year
2017
Product Type
Biologics
Center
CBER
Location
Chicago, IL (United States)