FDA Warning Letter — Sreedhar Samudrala

Case 413699 — FEI 3010026564

The FDA took a Warning Letter action against Sreedhar Samudrala on November 19, 2013 (Franklin, TN). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Sreedhar Samudrala
Date
November 19, 2013
Fiscal Year
2014
Product Type
Drugs
Center
CDER
Location
Franklin, TN (United States)