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483 Tedor Pharma, Nov 2007

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by Michelle Noe FDA

FDA investigators audited the Tedor Pharma - Cumberland , RI, United States facility and issued inspectional observation (via FDA 483) on 08 Nov 2007.

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Product Details

  • Inspection end: 08 Nov 2007
  • Location: Cumberland, United States
  • FEI: 3003855180
Tedor Pharma FDA inspection 483 Nov 2007

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