# FDA Inspection 999636 - VH Technologies Ltd. - February 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/vh-technologies-ltd/822989a0-9034-43da-aa7c-7bedcc0746e7
Source feed: FDA_Inspections

> FDA Inspection 999636 for VH Technologies Ltd. on February 02, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 999636
- Company Name: VH Technologies Ltd.
- Inspection Date: 2017-02-02
- 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 999636 - 2017-02-02](https://www.keypedia.com/records/fda_inspections/vh-technologies-ltd/5b9df015-3eb7-4dbe-b26c-4d0f27b3bca4)

Company: https://www.keypedia.com/companies/vh-technologies-ltd/bf902d1e-2e6f-4a25-a8b0-fe79ef641af7

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