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FDA Inspection 798912 — Keystone Laboratories, Inc.

Keystone Laboratories, Inc. — FEI 1020139

The FDA completed an inspection of Keystone Laboratories, Inc. on August 29, 2012 in Memphis, TN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 29, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Memphis, TN (United States)

Facility

Other inspections at this facility

  • 1038087 (OAI Thu Nov 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984429 (OAI Fri Feb 05 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 917925 (VAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 897322 (OAI Fri Sep 12 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 846286 (OAI Thu Aug 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources