# FDA Inspection 987864 - E-Teng Technology, Inc. - July 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/e-teng-technology-inc/074c85d5-e302-4b5c-97c2-755ebb2a8b72
Source feed: FDA_Inspections

> FDA Inspection 987864 for E-Teng Technology, Inc. on July 14, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987864
- Company Name: E-Teng Technology, Inc.
- Inspection Date: 2016-07-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1242306 - 2024-05-15](https://www.keypedia.com/records/fda_inspections/e-teng-technology-inc/a92e01f0-f853-4e19-b449-9348b2bbe850)
- [FDA Inspection 987864 - 2016-07-14](https://www.keypedia.com/records/fda_inspections/e-teng-technology-inc/130248c6-da45-4909-b1c9-3f0e0bd3c383)

Company: https://www.keypedia.com/companies/e-teng-technology-inc/d394885a-3ad0-445b-b089-6b74df4080a8

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