FDA inspection

Clinton River Medical Products, LLC: FDA inspection ending Sep 8, 2017

FDA inspection 1024836 · Voluntary Action Indicated (VAI) · Auburn Hills, MI

Key facts

Inspection ID 1024836
Firm Clinton River Medical Products, LLC
FEI number 3010376437
Address 1025 Doris Rd
City Auburn Hills
State MI
ZIP 48326
Country United States
Fiscal year 2017
Inspection end date Sep 8, 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

Browse all FDA inspections