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 3008790859.
Mixlab TX LLC
Weatherford, Texas, United States
Issue DateMarch 01, 2018
FEI Number3008790859
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Mixlab TX LLC FDA Form 483, Weatherford, Texas, March 1, 2018
