FDA Inspection
Aquila CorporationFDA Inspection 1224323 - Aquila Corporation - December 07, 2023
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Record Details
This FDA Inspection record concerns Aquila Corporation, with an inspection on December 7, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 5e5335f8-8b27-45dd-bad1-05c8da1236f7
Violation Codes4
21 CFR 801.20(a)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(g)
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