DashboardForm 483sForm 483 Details

Vericel Corporation Form 483 Details

Form 483
View FDA's record for this firm
Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3002836339.

Vericel Corporation

Cambridge, Massachusetts, United States
Issue DateAugust 21, 2009
FEI Number3002836339
CountryUnited States
Status
No Warning Letter
Product Type
Biologics
Vericel Corporation FDA Form 483, Cambridge, Massachusetts, August 21, 2009