FDA Warning Letter — Betty K. Tuller,Ph.D.

Case 224375 — FEI 3008231206

The FDA took a Warning Letter action against Betty K. Tuller,Ph.D. on December 12, 2011 (Arlington, VA). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Betty K. Tuller,Ph.D.
Date
December 12, 2011
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Arlington, VA (United States)