FDA WARNING_LETTER - Huaiyin Medical Instruments Co., Ltd. - April 02, 2009

FDA WARNING_LETTER for Huaiyin Medical Instruments Co., Ltd. on April 02, 2009. 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 Huaiyin Medical Instruments Co., Ltd. on April 02, 2009. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.250

21 CFR 820

21 U.S.C. 321(h)

21 U.S.C. 381(a)

21 CFR 803

21 CFR 820.75(a)

21 U.S.C. 351(h)

21 CFR 820.198(a)(3)

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

Huaiyin Medical Instruments Co., Ltd.

Inspection Date

April 2, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

People

Timothy A. Ulatowski (Director)

ID: 6b0b4852-c134-402f-8a3c-4441e4ae01ed

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