FDA Inspection 614275 — Keystone Pharmaceuticals Inc.

Keystone Pharmaceuticals Inc. — FEI 3006729542

The FDA completed an inspection of Keystone Pharmaceuticals Inc. on October 5, 2009 in Laguna Hills, CA. 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
October 5, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Laguna Hills, CA (United States)