FDA Inspection 999800 - Rentschler Biopharma SE - December 06, 2016

FDA Inspection 999800 for Rentschler Biopharma SE on December 06, 2016. Classification: Voluntary Action Indicated (VAI).

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 Inspection 999800 for Rentschler Biopharma SE on December 06, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.63

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

Rentschler Biopharma SE

Inspection Date

December 6, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fd3c2655-b57f-4166-9399-c3a17930da99

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