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 3016458098.
Walfer Corporation dba Wallace Pharmacy
Port Charlotte, Florida, United States
Issue DateMarch 16, 2020
FEI Number3016458098
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile and Non Sterile Drug Products
Sub Systems Impacted
2
Contamination ControlMedia Fill
Quality Systems
Facilities & Equipment
Walfer Corporation dba Wallace Pharmacy FDA Form 483, Port Charlotte, Florida, March 16, 2020
