# Full Power AED LLC – FDA Inspection, Dec 14, 2018

Source: https://www.keypedia.com/records/fda_inspections/full-power-aed-llc/fceca7a0-1f74-4964-9ca9-c752b33c3ed5
Source feed: FDA_Inspections

> FDA inspection 1074420 of Full Power AED LLC, December 14, 2018. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1074420
- Company Name: Full Power AED LLC
- Inspection Date: 2018-12-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

Company: https://www.keypedia.com/companies/full-power-aed-llc/091805b3-c489-4004-941e-9efe45e12fa4

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