Orca1

FDA inspection

Meridian Medical Technologies, Inc. a Pfizer Company: FDA inspection ending Jun 6, 2019

FDA inspection 1092063 · Official Action Indicated (OAI) · Brentwood, MO

Key facts

Inspection ID 1092063
Firm Meridian Medical Technologies, Inc. a Pfizer Company
FEI number 1950222
Address 2555 Hermelin Dr
City Brentwood
State MO
ZIP 63144
Fiscal year 2019
Inspection end date Jun 6, 2019
Classification Official Action Indicated (OAI)
Project area Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance
Product type Devices, Drugs

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

Other inspections at this establishment

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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