FDA issued a Warning Letter to Phillips Co. on 5/8/2017 as a result of this inspection.
FDA investigators audited the Phillips - Millerton, OK, United States facility and issued inspectional observations (via FDA 483) on 07 Oct 2016.
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- Category: Human Drugs
- Inspection end: 07 Oct 2016
- Location: Millerton, United States
- FEI: 3006899835