FDA inspection

Columbus Canvas Products: FDA inspection ending Sep 25, 2019

FDA inspection 1105956 · No Action Indicated (NAI) · Columbus, OH

Key facts

Inspection ID 1105956
Firm Columbus Canvas Products
FEI number 3009410520
Address 577 N 4th St
City Columbus
State OH
ZIP 43215
Country United States
Fiscal year 2019
Inspection end date Sep 25, 2019
Classification No Action Indicated (NAI)
Project area Compliance: 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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