FDA WARNING_LETTER - MASIMO CORPORATION - October 03, 2013

FDA WARNING_LETTER for MASIMO CORPORATION on October 03, 2013. 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 MASIMO CORPORATION on October 03, 2013. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 803.3

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.100(a)(2)

21 CFR 820.198(c)

21 CFR 803

21 U.S.C. 351(h)

21 CFR 820.100(a)(3)

21 CFR 820.198(e)

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

MASIMO CORPORATION

Inspection Date

October 3, 2013

Product Type

Devices

Office

Los Angeles District Office

People

ID: 20df8095-75f3-48e2-823f-e4e039f1585b

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