FDA Inspection 1015055 - Diasol, Inc - June 21, 2017

Record Details

This FDA Inspection record concerns Diasol, Inc, with an inspection on June 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Diasol, Inc
Inspection Date: June 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · de80a93e-8a77-4ff5-b9ab-d55008478ff7

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.198(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(a)21 CFR 820.30(f)21 CFR 820.30(j)21 CFR 820.40(a)

Full citation text and observation details available on the Dashboard.