Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3003436217.
ImprimisRx CA, Inc., dba ImprimisRx
Irvine, California, United States
Issue DateSeptember 01, 2016
FEI Number3003436217
CountryUnited States
Status
1 Related Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
ImprimisRx CA, Inc., dba ImprimisRx FDA Form 483, Irvine, California, September 1, 2016
