# FDA Inspection 1216778 - ECTOSENSE NV - August 31, 2023

Source: https://www.keypedia.com/records/fda_inspections/ectosense-nv/bdaf415a-e33b-4359-b082-fae9285b961d
Source feed: FDA_Inspections

> FDA Inspection 1216778 for ECTOSENSE NV on August 31, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216778
- Company Name: ECTOSENSE NV
- Inspection Date: 2023-08-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1216778 - 2023-08-31](https://www.keypedia.com/records/fda_inspections/ectosense-nv/37090dc6-a3d3-4f4e-986b-817e118aa075)

Company: https://www.keypedia.com/companies/ectosense-nv/180d04a7-b0b0-4641-8086-b845a640492d

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