FDA inspection

AED Battery Exchange LLC: FDA inspection ending Jun 26, 2017

FDA inspection 1015540 · Voluntary Action Indicated (VAI) · Wauconda, IL

Key facts

Inspection ID 1015540
Firm AED Battery Exchange LLC
FEI number 3009886119
Address 1000 Brown St Ste 206
City Wauconda
State IL
ZIP 60084
Country United States
Fiscal year 2017
Inspection end date Jun 26, 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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