FDA Inspection 984429 — Keystone Laboratories, Inc.

Keystone Laboratories, Inc. — FEI 1020139

The FDA completed an inspection of Keystone Laboratories, Inc. on February 5, 2016 in Memphis, TN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 5, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Memphis, TN (United States)

Citations

IDCFRDescription
188321 CFR 211.165(a)Testing and release for distribution
191221 CFR 211.166(a)Written program not followed
192021 CFR 211.166(a)(3)Valid stability test methods