FDA issued a Warning Letter to Pajunk GmbH on 11/17/2004 for a previous inspection.
483 Pajunk Jan 2013

483 Pajunk Jan 2013

Frank Marciniak FDA$119.00 - Available Now

FDA investigators audited the Pajunk - Geisingen, Germany facility and issued inspectional observations (via FDA 483) on 31 Jan 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 31 Jan 2013
  • Location: Geisingen, Germany
  • FEI: 3002807847
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