FDA Inspection 987018 - Shi Heng Technology Co., Ltd. - August 25, 2016

View on Dashboard

Discuss this record with AI

ChatGPT

Claude

Perplexity

Grok

Record Details

This FDA Inspection record concerns Shi Heng Technology Co., Ltd., with an inspection on August 25, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Shi Heng Technology Co., Ltd.
Inspection Date: August 25, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · d4d24de9-2e08-4e8d-8a64-b75281e64f76

Violation Codes10

21 CFR 803.17(b)(1)21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.20(c)21 CFR 820.25(b)21 CFR 820.30(e)21 CFR 820.50(a)(3)21 CFR 820.70(a)21 CFR 820.75(a)21 CFR 820.80(a)

Full citation text and observation details available on the Dashboard.