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483 Remel, Nov 2019

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by Rosanna Goodrich FDA

FDA investigators audited the Remel - Oakwood Village , OH, United States facility and issued inspectional observations (via FDA 483) on 20 Nov 2019.

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Product Details

  • Category: Medical Devices & Rad Health
  • Inspection end: 20 Nov 2019
  • Location: Oakwood Village, United States
  • FEI: 1000515493
Remel FDA inspection 483 Nov 2019

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