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 3027129265.
Nanjing Chengong Pharmaceutical Co., Ltd.
Nanjing, China
Issue DateMarch 21, 2025
FEI Number3027129265
CountryChina
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Drug Manufacturer
Nanjing Chengong Pharmaceutical Co., Ltd. FDA Form 483, Nanjing, March 21, 2025
