FDA inspection

MediBeacon, Inc: FDA inspection ending Aug 24, 2023

FDA inspection 1216964 · Voluntary Action Indicated (VAI) · Saint Louis, MO

Key facts

Inspection ID 1216964
Firm MediBeacon, Inc
FEI number 3027576156
Address 425 N New Ballas Rd Ste 100
City Saint Louis
State MO
ZIP 63141-6845
Fiscal year 2023
Inspection end date Aug 24, 2023
Classification Voluntary Action Indicated (VAI)
Project area Product Evaluation: Medical Devices
Product type Devices

At a glance

  • None 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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