FDA issued a Warning Letter to PlasmaCare, Inc. on 10/26/2007 for a previous inspection.
483 Grifols Biomat USA Aug 2017

483 Grifols Biomat USA Aug 2017

Amy Amaro FDA, La-Tasha Gunter FDA, Amy Johnson FDA$595.00 - Available Now

FDA investigators audited the Grifols Biomat USA - Richmond, VA, United States facility and issued inspectional observations (via FDA 483) on 31 Aug 2017.

Product details

  • Category: Biologics
  • Inspection end: 31 Aug 2017
  • Location: Richmond, United States
  • FEI: 3005523333
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