Source: FDA, document on file. FDA 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3010876031.
Observations12
Issue DateMay 04, 2018
StatusNo Warning Letter
Establishment TypeManufacturer
Related Inspections0
Establishment Details
Firm
Nutripack LLC
Location
Illinois, United States
FEI Number
3010876031
Establishment Type
Manufacturer
Product Type
Drugs
Issue Date
May 04, 2018
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.