FDA issued a Warning Letter to Meridian Medical Technologies, Inc. a Pfizer Company on 9/5/2017 as a result of this inspection.
FDA investigators audited the Meridian Medical Technologies a Pfizer Company - Brentwood, MO, United States facility and issued inspectional observations (via FDA 483) on 24 Mar 2017.
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- Category: Human Drugs / Medical Devices & Rad Health
- Inspection end: 24 Mar 2017
- Location: Brentwood, United States
- FEI: 1950222