# FDA Inspection 1202513 - Netech Corp. - April 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/netech-corp/936a524c-20ca-48bb-a3a6-688dbb136025
Source feed: FDA_Inspections

> FDA Inspection 1202513 for Netech Corp. on April 14, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1202513
- Company Name: Netech Corp.
- Inspection Date: 2023-04-14
- 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 1202513 - 2023-04-14](https://www.keypedia.com/records/fda_inspections/netech-corp/967fc882-5807-4479-bd37-736303d1f38f)
- [FDA Inspection 1106387 - 2019-10-08](https://www.keypedia.com/records/fda_inspections/netech-corp/657cebba-4e46-47f9-873f-5b42cee120cd)
- [FDA Inspection 1106387 - 2019-10-08](https://www.keypedia.com/records/fda_inspections/netech-corp/2b1343c6-dffb-4bea-9ac7-76aa607c0283)
- [FDA Inspection 979022 - 2016-06-16](https://www.keypedia.com/records/fda_inspections/netech-corp/5bb2e16b-cc53-4d54-ad6c-e12c1dab4910)
- [FDA Inspection 979022 - 2016-06-16](https://www.keypedia.com/records/fda_inspections/netech-corp/7247a686-e3a2-423d-b51c-d4555488c443)

Company: https://www.keypedia.com/companies/netech-corp/ec4307e9-5436-47cd-8ef8-ce55d364ed8d

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