# FDA Inspection 1100442 - Hummingbird Med Devices, Inc. - August 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/hummingbird-med-devices-inc/54424865-eda7-450a-b971-6dac31cc6cb9
Source feed: FDA_Inspections

> FDA Inspection 1100442 for Hummingbird Med Devices, Inc. on August 26, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100442
- Company Name: Hummingbird Med Devices, Inc.
- Inspection Date: 2019-08-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100442 - 2019-08-26](https://www.keypedia.com/records/fda_inspections/hummingbird-med-devices-inc/f6286049-d2af-4655-b92b-4819fa43039c)

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