FDA Inspection 1270505 - Baylab USA, LLC - May 20, 2025

FDA Inspection 1270505 for Baylab USA, LLC on May 20, 2025. Classification: Official Action Indicated (OAI).

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 1270505 for Baylab USA, LLC on May 20, 2025. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 801.20(a)

21 CFR 803.17

21 CFR 820.22

21 CFR 820.30(a)

21 CFR 820.50

21 CFR 830.310(b)

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

Baylab USA, LLC

Inspection Date

May 20, 2025

Product Type

Devices

ID: e24a2890-8d64-47b1-9eda-d445f7d01aec

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