FDA inspection

Amarex Clinical Research, LLC: FDA inspection ending Jan 11, 2010

FDA inspection 637968 · No Action Indicated (NAI) · Germantown, MD

Key facts

Inspection ID 637968
Firm Amarex Clinical Research, LLC
FEI number 3007940998
Address 20201 Century Blvd Fl 4
City Germantown
State MD
ZIP 20874
Country United States
Fiscal year 2010
Inspection end date Jan 11, 2010
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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