FDA issued a Warning Letter to Meridian Medical Technologies, Inc. a Pfizer Company on 9/5/2017 for a previous inspection.
483 Meridian Medical Technologies dba Meridian Medical Tec Dec 2019

483 Meridian Medical Technologies dba Meridian Medical Tec Dec 2019

Robert Ham FDA, Matthew Ondeck FDA, Eric Padgett FDA, Joseph Strelnik 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 21 Dec 2019.

Product details

  • Category: Human Drugs / Medical Devices & Rad Health
  • Inspection end: 21 Dec 2019
  • Location: Brentwood, United States
  • FEI: 1950222
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