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 3004575449.
PCI San Diego, Inc.
San Diego, California, United States
Issue DateJanuary 16, 2023
FEI Number3004575449
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Sterile Drug Manufacturer
PCI San Diego, Inc. FDA Form 483, San Diego, California, January 16, 2023
