FDA Inspection 678730 - Arbor Pharmaceuticals Inc. - August 27, 2010

FDA Inspection 678730 for Arbor Pharmaceuticals Inc. on August 27, 2010. 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 678730 for Arbor Pharmaceuticals Inc. on August 27, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.166(a)

21 CFR 211.198(a)

21 CFR 211.22(d)

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

Arbor Pharmaceuticals Inc.

Inspection Date

August 27, 2010

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fc62e7df-c76d-4b5a-9b87-5b0dde5a53b0

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