# Alung Technologies Inc – FDA Inspection, Mar 16, 2017

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

> FDA inspection 1016272 of Alung Technologies Inc, March 16, 2017. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## Related Documents

- FDA Inspection 1088940 - 2019-04-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/dennis-r-hock/f13e2db1-b808-466d-a974-e5af2d5dfdb0)

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

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