FDA Inspection 1109206 - KBD, Inc. - November 08, 2019

View on Dashboard

Discuss this record with AI

ChatGPT

Claude

Perplexity

Grok

Record Details

This FDA Inspection record concerns KBD, Inc., with an inspection on November 8, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: KBD, Inc.
Inspection Date: November 8, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · 01ca283d-b12b-47a0-8048-fd859e8d83c5

Violation Codes10

21 CFR 1010.2(b)21 CFR 1010.3(a)(2)(ii)21 CFR 1040.20(d)(1)(i)21 CFR 1040.20(d)(2)(iii)21 CFR 820.100(a)21 CFR 820.18121 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(i)

Full citation text and observation details available on the Dashboard.