# FDA Inspection 803591 - Elixir Research LLC - October 11, 2012

Source: https://www.keypedia.com/records/fda_inspections/elixir-research-llc/edefc6c2-91b6-449e-a325-c19f81098262
Source feed: FDA_Inspections

> FDA Inspection 803591 for Elixir Research LLC on October 11, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803591
- Company Name: Elixir Research LLC
- Inspection Date: 2012-10-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 803591 - 2012-10-11](https://www.keypedia.com/records/fda_inspections/elixir-research-llc/b4128127-3815-4e77-83a3-b25ca7b00434)

Company: https://www.keypedia.com/companies/elixir-research-llc/fc733f07-9655-4215-b661-e8a36d6e601b

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