# Bien-Air Surgery SA – FDA Inspection, Feb 16, 2023

Source: https://www.keypedia.com/records/fda_inspections/bien-air-surgery-sa/d8b01cd5-a25f-41fb-a8b6-081e3eb61bda
Source feed: FDA_Inspections

> FDA inspection 1198001 of Bien-Air Surgery SA, February 16, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 803. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1198001
- Company Name: Bien-Air Surgery SA
- Inspection Date: 2023-02-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1063812 - 2018-08-30](https://www.keypedia.com/records/fda_inspections/bien-air-surgery-sa/bbcca4e2-62e9-40e5-93c7-26d7343be331)
- [FDA Inspection 803507 - 2012-09-06](https://www.keypedia.com/records/fda_inspections/bien-air-surgery-sa/38b33ad5-c960-44f6-9b50-bfefe0df8cdd)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/juanj-wu/0d3e8970-b524-49f6-a307-079091b3c91d)

Company: https://www.keypedia.com/companies/bien-air-surgery-sa/e1a90f17-f666-46d9-b390-5d8e0e78a5b9

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