# Pulse Biomedical Inc – FDA Inspection, Nov 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/pulse-biomedical-inc/a76e77f2-1c12-43c2-a18d-885a67ca3785
Source feed: FDA_Inspections

> FDA inspection 1030842 of Pulse Biomedical Inc, November 06, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030842
- Company Name: Pulse Biomedical Inc
- Inspection Date: 2017-11-06
- 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: 1

## Related Documents

- FDA Inspection 915470 - 2015-03-05
- FDA Inspection 808339 - 2012-10-23
- FDA Inspection 601767 - 2009-07-16

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/edward-d-mcdonald/69224613-2b96-426a-99dd-e1cfe5ff1713)

Company: https://www.keypedia.com/companies/pulse-biomedical-inc/1f1e83c4-ecde-48a6-b83b-039cfce6f0c2

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