FDA WARNING_LETTER - Je Dois Lavoir LLC - August 11, 2021

FDA WARNING_LETTER for Je Dois Lavoir LLC on August 11, 2021. 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 Je Dois Lavoir LLC on August 11, 2021. Product: Drugs. Access full analysis and detailed observations.

Violation Codes

21 U.S.C. 331(d)

21 U.S.C. 352(j)

21 U.S.C. 321(p)

21 U.S.C. 321(n)

21 U.S.C. 331(a)

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

21 U.S.C. 352(a)

21 U.S.C. 352(f)(2)

21 U.S.C. 502

21 CFR 201.100(c)(2)

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

Je Dois Lavoir LLC

Inspection Date

August 11, 2021

Product Type

Drugs

Office

Division of Pharmaceutical Quality Operations IV

People

Lance M. De Souza (Director - Compliance Branch)

ID: 996ca43d-65b0-4428-b946-171e873beef1

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