# FDA Inspection 1230336 - Kaleo, Inc. - February 29, 2024

Source: https://www.keypedia.com/records/fda_inspections/kaleo-inc/9e2e91e4-6165-467a-9958-eaf22ba92691
Source feed: FDA_Inspections

> FDA Inspection 1230336 for Kaleo, Inc. on February 29, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1230336
- Company Name: Kaleo, Inc.
- Inspection Date: 2024-02-29
- 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 1230336 - 2024-02-29](https://www.keypedia.com/records/fda_inspections/kaleo-inc/279aec33-1bf2-4c3b-97eb-840dd8e14d16)
- [FDA Inspection 1099882 - 2019-07-31](https://www.keypedia.com/records/fda_inspections/kaleo-inc/d998892b-b87f-414c-bb10-ade75d26e549)
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- [FDA Inspection 731834 - 2011-06-27](https://www.keypedia.com/records/fda_inspections/kaleo-inc/71e50312-318a-4d62-b799-81d67b7d0507)

Company: https://www.keypedia.com/companies/kaleo-inc/848a3c90-81e0-442c-9c0a-be42352217a5

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