483 Kessel Medintim Gmbh Nov 2017

483 Kessel Medintim Gmbh Nov 2017

Seema Singh FDA$119.00 - Available Now

FDA investigators audited the Kessel Medintim Gmbh - Morfelden-Walldorf, Germany facility and issued inspectional observations (via FDA 483) on 02 Nov 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 02 Nov 2017
  • Location: Morfelden-Walldorf, Germany
  • FEI: 3011014178
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