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 3005946041.
Mixlab WI LLC
Milwaukee, Wisconsin, United States
Issue DateAugust 07, 2018
FEI Number3005946041
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Non Sterile Drug Products
Mixlab WI LLC FDA Form 483, Milwaukee, Wisconsin, August 7, 2018
