# IntelleWave, Inc. – FDA Inspection, Aug 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/intellewave-inc/6a9174c4-313a-4749-9d9d-9e2103700391
Source feed: FDA_Inspections

> FDA inspection 1020784 of IntelleWave, Inc., August 02, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020784
- Company Name: IntelleWave, Inc.
- Inspection Date: 2017-08-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1237790 - 2024-04-25

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/intellewave-inc/77dd1263-9e8d-4924-9f19-5ca88ef1849c

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