# Electronic Waveform Lab, Inc. – FDA Inspection, Feb 8, 2018

Source: https://www.keypedia.com/records/fda_inspections/electronic-waveform-lab-inc/0deee1bf-80a5-4b88-97f4-cde43fe53720
Source feed: FDA_Inspections

> FDA inspection 1040264 of Electronic Waveform Lab, Inc., February 08, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040264
- Company Name: Electronic Waveform Lab, Inc.
- Inspection Date: 2018-02-08
- 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: 4

## Related Documents

- FDA Inspection 1196109 - 2023-01-11
- FDA Inspection 794748 - 2012-08-06

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

Company: https://www.keypedia.com/companies/electronic-waveform-lab-inc/b497cd0e-ddf2-44b8-ad08-657d88430bc7

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