FDA WARNING_LETTER - Trilogy Laboratories, LLC - August 27, 2019

FDA WARNING_LETTER for Trilogy Laboratories, LLC on August 27, 2019. Product: Drugs. 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 Trilogy Laboratories, LLC on August 27, 2019. Product: Drugs. Access full analysis and detailed observations.

Violation Codes

21 CFR 211.100(a)

21 U.S.C. 331(d)

21 U.S.C. 321(p)

21 CFR 201.66

21 CFR 330.1

21 CFR 201.61

21 U.S.C. 331(a)

21.U.S.C. 355(a)

21 U.S.C. 352(a)

21 CFR 211

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

Trilogy Laboratories, LLC

Inspection Date

August 27, 2019

Product Type

Drugs

Office

Office of Pharmaceutical Quality Operations Division I

People

ID: ae30ca41-88f8-41ef-a662-4ae79761a6b8

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