FDA WARNING_LETTER - Jiangsu JDC Medical Devices Co., Ltd. - September 19, 2019

FDA WARNING_LETTER for Jiangsu JDC Medical Devices Co., Ltd. on September 19, 2019. Product: Devices. Access full analysis and detailed observations.

View on Dashboard

One-time purchase from the GKS catalog. Lifetime access in your library. Single documents and full company profiles available. All sales final.

Record Summary

FDA WARNING_LETTER for Jiangsu JDC Medical Devices Co., Ltd. on September 19, 2019. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.120

21 U.S.C. 352(t)(2)

21 CFR 820.30(a)

21 CFR 820.70(c)

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.70(a)

21 U.S.C. 381(a)

21 CFR 803

21 U.S.C. 351(h)

Get More Insights

Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.

1.5M+ regulatory data points

Real-time compliance monitoring

Interactive analytics dashboard

Looking for more records? Our platform provides access to thousands of similar regulatory documents with advanced search and filtering capabilities.

Record Information

Company

Jiangsu JDC Medical Devices Co., Ltd.

Inspection Date

September 19, 2019

Product Type

Devices

Office

Office of Health Technology 3 (Gastrorenal, ObGyn, General Hospital, and Urology Devices)

People

ID: 970078a5-2ac0-4700-8f92-964c54b176a6

View on Dashboard

Transform Regulatory Data into Actionable Intelligence

Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.

Try KeyPedia Today

Explore our real use cases and discover our features in depth.

Subscribe to our newsletter

Get the latest updates and insights delivered to your inbox