483 Tedor Pharma Nov 2007

483 Tedor Pharma Nov 2007

Michelle Noe FDA$119.00 - Available Now

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

Product details

  • Category: Human Drugs
  • Inspection end: 08 Nov 2007
  • Location: Cumberland, United States
  • FEI: 3003855180
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