FDA Inspection 1009111 — Aruba Aloe Balm N.V.

Aruba Aloe Balm N.V. — FEI 3004117460

The FDA completed an inspection of Aruba Aloe Balm N.V. on Mar 22, 2017 in Oranjestad. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oranjestad (Aruba)

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