# FDA Inspection 1074420 - Full Power AED LLC - December 14, 2018

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

> FDA Inspection 1074420 for Full Power AED LLC on December 14, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

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

## Related Documents

- [FDA Inspection 1074420 - 2018-12-14](https://www.globalkeysolutions.net/api/records/fda_inspections/full-power-aed-llc/c6700739-6e8e-4cbc-ba78-5dd7b8497bcf/)

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

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