FDA Inspection 1157059 — AED Battery Exchange LLC

AED Battery Exchange LLC — FEI 3009886119

The FDA completed an inspection of AED Battery Exchange LLC on Nov 8, 2021 in Wauconda, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 8, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Wauconda, IL (United States)

Additional Details

Postmarket Audit Inspections

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.