483 Remel Mar 2010

483 Remel Mar 2010

Laureen Geniusz FDA$119.00 - Available Now

FDA investigators audited the Remel - Oakwood Village, OH, United States facility and issued inspectional observations (via FDA 483) on 16 Mar 2010.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 16 Mar 2010
  • Location: Oakwood Village, United States
  • FEI: 1000515493
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