FDA Inspection 1086925 - KJK Enterprise, Inc. - February 22, 2019

FDA Inspection 1086925 for KJK Enterprise, Inc. on February 22, 2019. Classification: Voluntary Action Indicated (VAI).

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 1086925 for KJK Enterprise, Inc. on February 22, 2019. Classification: Voluntary Action Indicated (VAI).

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

KJK Enterprise, Inc.

Inspection Date

February 22, 2019

Product Type

Food/Cosmetics

ID: f9d55403-74a2-4e85-846e-2294805e9a81

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