FDA Inspection 890363 — UBI Pharma, Inc.

UBI Pharma, Inc. — FEI 3004713402

The FDA completed an inspection of UBI Pharma, Inc. on July 18, 2014 in Hsinchu County. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 18, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hsinchu County (Taiwan)