FDA issued a Warning Letter to Cantrell Drug Company on 1/21/2015 for a previous inspection.
483 Cantrell Drug Company Aug 2018

483 Cantrell Drug Company Aug 2018

Bonita Chester FDA, Claire Minden FDA$119.00 - Available Now

FDA investigators audited the Cantrell Drug Company - Little Rock, AR, United States facility and issued inspectional observations (via FDA 483) on 22 Aug 2018.

Product details

  • Category: Human Drugs
  • Inspection end: 22 Aug 2018
  • Location: Little Rock, United States
  • FEI: 3004483441
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