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483 Vericel, May 2016

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by Simone Pitts FDA

FDA investigators audited the Vericel - Cambridge , MA, United States facility and issued inspectional observation (via FDA 483) on 27 May 2016.

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Product Details

  • Inspection end: 27 May 2016
  • Location: Cambridge, United States
  • FEI: 3002836339
Vericel FDA inspection 483 May 2016

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