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 3014549846.
OSRX Inc.
Missoula, Montana, United States
Issue DateApril 25, 2019
FEI Number3014549846
CountryUnited States
Status
1 Related Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
OSRX Inc. FDA Form 483, Missoula, Montana, April 25, 2019
