Safeway, Inc.June 12, 2017

FDA 483 - Safeway, Inc. - June 12, 2017

FDA 483 for Safeway, Inc. on June 12, 2017. Product: Drugs. Access full analysis and detailed observations.

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 483 for Safeway, Inc. on June 12, 2017. Product: Drugs. Access full analysis and detailed observations.

Violation Codes

21 U.S.C. 360(j)

FD&C Act 501(a)(2)(B)

21 CFR 211

21 CFR 210

21 U.S.C. 352(f)(1)

21 CFR 314.80(b)

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

Safeway, Inc.

Inspection Date

June 12, 2017

Product Type

Drugs

Office

Denver District Office

People

ID: 82d6f7ac-cac0-44c7-a700-60ef04b356b1

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