# FDA Inspection 1038662 - AOTI Ltd. - July 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/aoti-ltd/273ad460-fff4-477f-b21e-aee3e6c58503
Source feed: FDA_Inspections

> FDA Inspection 1038662 for AOTI Ltd. on July 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038662
- Company Name: AOTI Ltd.
- Inspection Date: 2017-07-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 661652 - 2010-04-22](https://www.keypedia.com/records/fda_inspections/aoti-ltd/286455d0-9386-48a7-b31c-467d548c71d7)

Company: https://www.keypedia.com/companies/aoti-ltd/2cf338d4-560c-4ebe-a4a5-1eb10d1c5e57

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