Source: FDA, document on file. FDA 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3021247180.
Observations5
Issue DateMay 30, 2025
StatusWarning Letter Issued
Establishment TypeDrug Manufacturer
Related Inspections0
Establishment Details
Firm
Capricor, Inc.
Location
California, United States
FEI Number
3021247180
Establishment Type
Drug Manufacturer
Issue Date
May 30, 2025
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.