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483 Remel, Apr 2017

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FDA investigators audited the Remel - Oakwood Village , OH, United States facility and issued inspectional observations (via FDA 483) on 12 Apr 2017.

Product Details

  • Category: Medical Devices & Rad Health
  • Inspection end: 12 Apr 2017
  • Location: Oakwood Village, United States
  • FEI: 1000515493
Remel FDA inspection 483 Apr 2017

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