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483 Response Artegraft, Jun 2003

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FDA investigators audited the Artegraft - North Brunswick , NJ, United States facility and issued inspectional observation (via FDA 483) on 10 Jun 2003.

Product Details

  • Inspection end: 10 Jun 2003
  • Location: North Brunswick, United States
  • FEI: 1000121696
Artegraft FDA inspection 483 Jun 2003

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