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 3003531601.
Michigan Medicine
Ann Arbor, Michigan, United States
Issue DateAugust 08, 2016
FEI Number3003531601
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Michigan Medicine FDA Form 483, Ann Arbor, Michigan, August 8, 2016
