FDA Inspection 1014057 — Albert Max, Inc.

Albert Max, Inc. — FEI 3004130952

The FDA completed an inspection of Albert Max, Inc. on May 25, 2017 in Chino, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 25, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chino, CA (United States)

Citations

IDCFRDescription
107921 CFR 211.22(a)Contract drug products--lack of responsibility
360321 CFR 211.160(b)Scientifically sound laboratory controls