483 Remel Jun 2013

483 Remel Jun 2013

Lori Gioia FDA, James Planchon FDA$119.00 - Available Now

FDA investigators audited the Remel - Lenexa, KS, United States facility and issued inspectional observations (via FDA 483) on 25 Jun 2013.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 25 Jun 2013
  • Location: Lenexa, United States
  • FEI: 1924669
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