FDA inspection

Meridian Medical Systems LLC: FDA inspection ending Feb 24, 2017

FDA inspection 1002415 · Voluntary Action Indicated (VAI) · Aurora, OH

Key facts

Inspection ID 1002415
Firm Meridian Medical Systems LLC
FEI number 3008492862
Address 325 Harris Dr
City Aurora
State OH
ZIP 44202
Country United States
Fiscal year 2017
Inspection end date Feb 24, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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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