FDA inspection

Apneicare LLC: FDA inspection ending May 5, 2015

FDA inspection 924046 · Voluntary Action Indicated (VAI) · Columbus, OH

Key facts

Inspection ID 924046
Firm Apneicare LLC
FEI number 3007799743
Address 985 Schrock Rd
City Columbus
State OH
ZIP 43229
Country United States
Fiscal year 2015
Inspection end date May 5, 2015
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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