FDA issued a Warning Letter to Ropack, Inc. on 8/3/2016 as a result of this inspection.
483 Ropack Jan 2016

483 Ropack Jan 2016

Ashley Mutawakkil FDA$119.00 - Available Now

FDA investigators audited the Ropack - Anjou, Canada facility and issued inspectional observations (via FDA 483) on 21 Jan 2016.

Product details

  • Category: Human Drugs / Medical Devices & Rad Health
  • Inspection end: 21 Jan 2016
  • Location: Anjou, Canada
  • FEI: 3002674295
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