# VH Technologies Ltd. – FDA Inspection, Feb 2, 2017

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

> FDA inspection 999636 of VH Technologies Ltd., February 02, 2017. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- 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: 12

## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

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