FDA Warning Letter — ImprimisRx CA, Inc., dba ImprimisRx

Case 509499 — FEI 3003436217

The FDA took a Warning Letter action against ImprimisRx CA, Inc., dba ImprimisRx on March 20, 2017 (Irvine, CA). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
ImprimisRx CA, Inc., dba ImprimisRx
Date
March 20, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Irvine, CA (United States)