FDA issued a Warning Letter to Meridian Medical Technologies, Inc. a Pfizer Company on 9/5/2017 as a result of this inspection.
483 Meridian Medical Technologies dba Meridian Medical Tec Mar 2017

483 Meridian Medical Technologies dba Meridian Medical Tec Mar 2017

Zedong Dong FDA, Rick Friedman FDA, Kellia Hicks FDA, John Mcmichael FDA, Michele Obert FDA, Phillip Pontikos FDA, Frank Wackes FDA$119.00 - Available Now

FDA investigators audited the Meridian Medical Technologies dba Meridian Medical Tec - Brentwood, MO, United States facility and issued inspectional observations (via FDA 483) on 24 Mar 2017.

Product details

  • Category: Human Drugs / Medical Devices & Rad Health
  • Inspection end: 24 Mar 2017
  • Location: Brentwood, United States
  • FEI: 1950222
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