FDA Inspection 756101 - Pur-Sleep Inc. - December 08, 2011

FDA Inspection 756101 for Pur-Sleep Inc. on December 08, 2011. 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 756101 for Pur-Sleep Inc. on December 08, 2011. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.20(e)

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

Pur-Sleep Inc.

Inspection Date

December 8, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff78ee39-abbe-4522-ba45-245352c73785

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