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 3007187671.
Observations1
Issue DateOctober 19, 2009
StatusNo Warning Letter
Establishment TypeDrug Manufacturer
Related Inspections0
Establishment Details
Firm
Matrixx Initiatives Inc.
Location
Arizona
FEI Number
3007187671
Establishment Type
Drug Manufacturer
Issue Date
October 19, 2009
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.