FDA issued a Warning Letter to Phillips Co. on 5/8/2017 as a result of this inspection.
483 Phillips Oct 2016

483 Phillips Oct 2016

Shawn Larson FDA$119.00 - Available Now

FDA investigators audited the Phillips - Millerton, OK, United States facility and issued inspectional observations (via FDA 483) on 07 Oct 2016.

Product details

  • Category: Human Drugs
  • Inspection end: 07 Oct 2016
  • Location: Millerton, United States
  • FEI: 3006899835
Add To Cart