# Longeviti Neuro Solutions LLC – FDA Inspection, Aug 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/longeviti-neuro-solutions-llc/4eac8a65-d0e0-4cab-be50-5a89f81faeee
Source feed: FDA_Inspections

> FDA inspection 1100438 of Longeviti Neuro Solutions LLC, August 26, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1100438
- Company Name: Longeviti Neuro Solutions LLC
- Inspection Date: 2019-08-26
- 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: 2

## Related Documents

- [FDA Inspection 1254554 - 2024-11-15](https://www.keypedia.com/records/fda_inspections/longeviti-neuro-solutions-llc/db83ea65-a0cf-4b9b-85b4-8b1ec4c15804)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/daniel-t-lee/8147e5b2-2065-42e3-b86c-36c0231f74cc)

Company: https://www.keypedia.com/companies/longeviti-neuro-solutions-llc/3d3766f2-9c63-4002-b63e-c8843a8d28b7

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