# AQUISEL S.L.U. – FDA Inspection, May 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/aquisel-slu/6bd56066-0093-4b5c-8589-48d4a66562a6
Source feed: FDA_Inspections

> FDA inspection 1090088 of AQUISEL S.L.U., May 15, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1090088
- Company Name: AQUISEL S.L.U.
- Inspection Date: 2019-05-15
- 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 Officers

- [Investigator](https://www.keypedia.com/people/stephen-r-souza/9b7af4df-f1cc-468d-9761-cee11d3c14fc)

Company: https://www.keypedia.com/companies/aquisel-slu/ec24ebab-35c9-4aff-87da-d24b55eda4e7

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