FDA issued a Warning Letter to Actavis Totowa, LLC on 2/1/2007 for a previous inspection.
483 Actavis Totowa Mar 2009

483 Actavis Totowa Mar 2009

Douglas Kovacs FDA, Erin Mccaffery FDA$119.00 - Available Now

FDA investigators audited the Actavis Totowa - Little Falls, NJ, United States facility and issued 4 inspectional observations (via FDA 483) on 31 Mar 2009.

Product details

  • Category: Human Drugs
  • Number of Observations: 4
  • Inspection end: 31 Mar 2009
  • Location: Little Falls, United States
  • FEI: 2244683
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