# FDA Inspection 1090088 - AQUISEL S.L.U. - May 15, 2019

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

> FDA Inspection 1090088 for AQUISEL S.L.U. on May 15, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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