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FDA Inspection
•Aruba Aloe Balm N.V.•March 22, 2017

Aruba Aloe Balm N.V. – FDA Inspection, Mar 22, 2017

Record Details

This FDA Inspection record concerns Aruba Aloe Balm N.V., with an inspection on March 22, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Aruba Aloe Balm N.V.
Inspection Date
March 22, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jose A. Cruz Gonzalez
View Company Profile

ID · f7d2535b-13a9-437b-85aa-dc5d04f9d1e1

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1009111
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Aruba Aloe Balm N.V.

1
DateClassificationOfficeProject area
November 16, 2023OAIDrug Quality Assurance
Other documents for Aruba Aloe Balm N.V.
  • FDA Inspection 1225306 - 2023-11-16

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