FDA inspection

Medbio, Inc.: FDA inspection ending Aug 22, 2016

FDA inspection 981666 · No Action Indicated (NAI) · Grand Rapids, MI

Key facts

Inspection ID 981666
Firm Medbio, Inc.
FEI number 3009810261
Address 5346 36th St Se
City Grand Rapids
State MI
ZIP 49512
Country United States
Fiscal year 2016
Inspection end date Aug 22, 2016
Classification No Action Indicated (NAI)
Project area Project Evaluation: Devices
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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