FDA Warning Letter — Janet K Tillisch, MD

Case 398635 — FEI 3010098837

The FDA took a Warning Letter action against Janet K Tillisch, MD on June 20, 2013 (Fargo, ND). The action was issued by CBER and concerns biologics products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Janet K Tillisch, MD
Date
June 20, 2013
Fiscal Year
2013
Product Type
Biologics
Center
CBER
Location
Fargo, ND (United States)