FDA inspection

Ranir, LLC: FDA inspection ending Aug 16, 2017

FDA inspection 1021914 · Voluntary Action Indicated (VAI) · Grand Rapids, MI

Key facts

Inspection ID 1021914
Firm Ranir, LLC
FEI number 1825660
Address 4701 E Paris Ave SE
City Grand Rapids
State MI
ZIP 49512
Country United States
Fiscal year 2017
Inspection end date Aug 16, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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