FDA inspection

Curbell Medical Products, Inc.: FDA inspection ending Mar 27, 2017

FDA inspection 1006300 · Voluntary Action Indicated (VAI) · Orchard Park, NY

Key facts

Inspection ID 1006300
Firm Curbell Medical Products, Inc.
FEI number 3000210521
Address 20 Centre Dr
City Orchard Park
State NY
ZIP 14127
Country United States
Fiscal year 2017
Inspection end date Mar 27, 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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