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 Jun 2019

483 Meridian Medical Technologies dba Meridian Medical Tec Jun 2019

Sandra Boyd FDA, Rick Friedman FDA, Robert Ham FDA, Rohit Kolhatkar FDA, Edward Lockwood FDA, Matthew Ondeck FDA, Phillip Pontikos FDA, Alex Viehmann FDA, Sandra Hughes 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 06 Jun 2019.

Product details

  • Category: Human Drugs / Medical Devices & Rad Health
  • Inspection end: 06 Jun 2019
  • Location: Brentwood, United States
  • FEI: 1950222
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