# AED Battery Exchange LLC – FDA Inspection, Jun 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/aed-battery-exchange-llc/b800d221-f2dc-4946-b935-45e7972bd44f
Source feed: FDA_Inspections

> FDA inspection 1015540 of AED Battery Exchange LLC, June 26, 2017. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015540
- Company Name: AED Battery Exchange LLC
- Inspection Date: 2017-06-26
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1312226 - 2026-04-09](https://www.keypedia.com/records/fda_inspections/aed-battery-exchange-llc/f6a817d7-807f-4d08-9c20-eac294091992)
- FDA Inspection 1157059 - 2021-11-08
- FDA Inspection 818386 - 2013-02-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/david-j-gasparovich/478888db-d4b3-481a-89f5-ee234a160f07)

Company: https://www.keypedia.com/companies/aed-battery-exchange-llc/12b427c9-efc4-4ba6-8f82-0247f692ac17

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
