FDA issued a Warning Letter to Sopro Comeg Gmbh on 2/23/2015 as a result of this inspection.
483 Sopro Comeg Gmbh May 2014

483 Sopro Comeg Gmbh May 2014

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FDA investigators audited the Sopro Comeg Gmbh - Tuttlingen, Germany facility and issued inspectional observations (via FDA 483) on 08 May 2014.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 08 May 2014
  • Location: Tuttlingen, Germany
  • FEI: 3005840432
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