# Hummingbird Med Devices, Inc. – FDA Inspection, Aug 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/hummingbird-med-devices-inc/f6286049-d2af-4655-b92b-4819fa43039c
Source feed: FDA_Inspections

> FDA inspection 1100442 of Hummingbird Med Devices, Inc., August 26, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100442
- Company Name: Hummingbird Med Devices, Inc.
- Inspection Date: 2019-08-26
- 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: 2

## Related Officers

- [Investigator](https://www.keypedia.com/people/stephen-r-souza/9b7af4df-f1cc-468d-9761-cee11d3c14fc)

Company: https://www.keypedia.com/companies/hummingbird-med-devices-inc/5b471ed7-ad89-4825-971c-ba9d43a0401a

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