# FDA Inspection 1224982 - Amplivox Ltd - December 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/amplivox-ltd/10442d81-6cd9-44ca-be3e-90f0aa1a6fd3
Source feed: FDA_Inspections

> FDA Inspection 1224982 for Amplivox Ltd on December 14, 2023. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1224982
- Company Name: Amplivox Ltd
- Inspection Date: 2023-12-14
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1224982 - 2023-12-14](https://www.keypedia.com/records/fda_inspections/amplivox-ltd/6e1c3b30-29ca-4a31-be68-5449bcfa7a38)
- [FDA Inspection 761210 - 2011-12-15](https://www.keypedia.com/records/fda_inspections/amplivox-ltd/d499ccbe-2710-4d1b-bcd4-d8114ed7b4fe)
- [FDA Inspection 761210 - 2011-12-15](https://www.keypedia.com/records/fda_inspections/amplivox-ltd/7b07e148-7d90-455c-bb8c-3a9aef775302)

Company: https://www.keypedia.com/companies/amplivox-ltd/a916a18f-7deb-4223-8dc9-fa0998ee388a

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