FDA EIR - Bio-Thesiometer USA - January 19, 2018

FDA EIR for Bio-Thesiometer USA on January 19, 2018. Product: devices. Access full analysis and detailed observations.

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 EIR for Bio-Thesiometer USA on January 19, 2018. Product: devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.180

21 CFR 820.198

21 CFR 820.30

21 CFR 820

21 CFR 820.198(a)

21 CFR 803

21 CFR 882.1200

21 CFR 803.17

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

Bio-Thesiometer USA

Inspection Date

January 19, 2018

Product Type

devices

Office

Food and Drug Administration

People

ID: e86e2680-bf02-478f-8aa7-e496bbf41cde

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