# FDA Inspection 947350 - Suzhou Armocon Technology Co.Ltd - September 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/suzhou-armocon-technology-coltd/58bbb206-2d06-4b5a-932f-1d9bfe73db63
Source feed: FDA_Inspections

> FDA Inspection 947350 for Suzhou Armocon Technology Co.Ltd on September 17, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 947350
- Company Name: Suzhou Armocon Technology Co.Ltd
- Inspection Date: 2015-09-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 947350 - 2015-09-17](https://www.keypedia.com/records/fda_inspections/suzhou-armocon-technology-coltd/02d3533c-657b-48b9-84a9-8572dd6d19cc)
- [FDA Inspection 841203 - 2013-07-11](https://www.keypedia.com/records/fda_inspections/suzhou-armocon-technology-coltd/7559d37f-07b3-4fe0-8bff-0089014216f9)
- [FDA Inspection 841203 - 2013-07-11](https://www.keypedia.com/records/fda_inspections/suzhou-armocon-technology-coltd/80cf1d42-3fc6-4c83-931e-f6ec3de1f6d3)

Company: https://www.keypedia.com/companies/suzhou-armocon-technology-coltd/5da0acc7-38f6-452f-a414-f946d1df71ec

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