# FDA Inspection 1234448 - Personal Genome Diagnostics Inc. - March 14, 2024

Source: https://www.keypedia.com/records/fda_inspections/personal-genome-diagnostics-inc/6a54a481-c51c-49e1-a3b5-9d56a3de7a4e
Source feed: FDA_Inspections

> FDA Inspection 1234448 for Personal Genome Diagnostics Inc. on March 14, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1234448
- Company Name: Personal Genome Diagnostics Inc.
- Inspection Date: 2024-03-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1303586 - 2026-02-13](https://www.keypedia.com/records/fda_inspections/personal-genome-diagnostics-inc/9f61f9bd-bb10-4a09-b0c8-5268879be2d0)
- [FDA Inspection 1234448 - 2024-03-14](https://www.keypedia.com/records/fda_inspections/personal-genome-diagnostics-inc/5b1f98b1-f5e7-4d60-9709-122239127588)

Company: https://www.keypedia.com/companies/personal-genome-diagnostics-inc/a5c4192b-6ea7-4b94-b1e8-84f07d5d8b83

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