# FDA Inspection 988220 - Elixir Corporation - September 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/elixir-corporation/98eb6eb4-7fce-4b33-a212-cc52b78656bf
Source feed: FDA_Inspections

> FDA Inspection 988220 for Elixir Corporation on September 15, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988220
- Company Name: Elixir Corporation
- Inspection Date: 2016-09-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1039236 - 2018-01-10](https://www.keypedia.com/records/fda_inspections/elixir-corporation/e098c99c-d778-471d-8dc3-f74f1ab4eb31)

Company: https://www.keypedia.com/companies/elixir-corporation/d11e80da-fe5b-48e8-bffb-4f20f049db42

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