# FDA Inspection 1099935 - Embolx, Inc. - July 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/embolx-inc/8b61e657-e008-4a02-baa2-b15ad27aa56b
Source feed: FDA_Inspections

> FDA Inspection 1099935 for Embolx, Inc. on July 25, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1099935
- Company Name: Embolx, Inc.
- Inspection Date: 2019-07-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195728 - 2023-01-19](https://www.keypedia.com/records/fda_inspections/embolx-inc/7656bcf0-a41f-44b2-8331-fab503d5c150)
- [FDA Inspection 1195728 - 2023-01-19](https://www.keypedia.com/records/fda_inspections/embolx-inc/5e4a7d3e-694a-457f-a9a4-c48bdb574203)
- [FDA Inspection 1099935 - 2019-07-25](https://www.keypedia.com/records/fda_inspections/embolx-inc/411d21a0-2a3c-4647-9429-ab7bf0d0c60a)

Company: https://www.keypedia.com/companies/embolx-inc/3d06d7b2-85d3-4016-a1dd-ec60b5d4c00b

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