FDA inspection

Mary Washington Hospital IRB: FDA inspection ending May 26, 2017

FDA inspection 1011857 · Voluntary Action Indicated (VAI) · Fredericksburg, VA

Key facts

Inspection ID 1011857
Firm Mary Washington Hospital IRB
FEI number 1122508
Address 1001 Sam Perry Blvd
City Fredericksburg
State VA
ZIP 22401-4453
Fiscal year 2017
Inspection end date May 26, 2017
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices
Product type Biologics, Devices, Drugs

At a glance

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

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

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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