FDA issued a Warning Letter to Curasan AG, Frankfurt Facility on 8/23/2017 as a result of this inspection.
483 Curasan AG, Frankfurt Facility May 2017

483 Curasan AG, Frankfurt Facility May 2017

Thai Duong FDA$119.00 - Available Now

FDA investigators audited the Curasan AG, Frankfurt Facility - Frankfurt am Main, Germany facility and issued inspectional observations (via FDA 483) on 11 May 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 11 May 2017
  • Location: Frankfurt am Main, Germany
  • FEI: 3004847139
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