# ECTOSENSE NV – FDA Inspection, Aug 31, 2023

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

> FDA inspection 1216778 of ECTOSENSE NV, August 31, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1216778
- Company Name: ECTOSENSE NV
- Inspection Date: 2023-08-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maryam-tabatabaie/b792042d-e296-446d-90a9-d30c8f635506)

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