# FDA Inspection 1016272 - Alung Technologies Inc - March 16, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/alung-technologies-inc/f6ceb5ae-fb2a-40d5-acd7-7e66457cb754/
Source feed: FDA_Inspections

> FDA Inspection 1016272 for Alung Technologies Inc on March 16, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016272
- Company Name: Alung Technologies Inc
- Inspection Date: 2017-03-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1088940 - 2019-04-03](https://www.globalkeysolutions.net/api/records/fda_inspections/alung-technologies-inc/b4cd4e76-e104-42bc-b2d3-4b55be35641f/)
- [FDA Inspection 1016272 - 2017-03-16](https://www.globalkeysolutions.net/api/records/fda_inspections/alung-technologies-inc/82d6816f-d8cc-4ebb-a587-338c3159a2dd/)

Company: https://www.globalkeysolutions.net/companies/alung-technologies-inc/5acae832-8383-49ff-b1cb-a17d769cce48

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