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

Record Details

This FDA Inspection record concerns AQUISEL S.L.U., with an inspection on May 15, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: AQUISEL S.L.U.
Inspection Date: May 15, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6bd56066-0093-4b5c-8589-48d4a66562a6

Violation Codes2

21 CFR 820.250(a)21 CFR 820.40(a)

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