FDA Inspection 1023661 — Onix Bodycare Products Factory

Onix Bodycare Products Factory — FEI 3006759180

The FDA completed an inspection of Onix Bodycare Products Factory on August 9, 2017 in Enping City. 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
August 9, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Enping City (China)