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FDA Inspection
•Aloe Vera of America, Inc•January 11, 2013

Aloe Vera of America, Inc – FDA Inspection, Jan 11, 2013

Record Details

This FDA Inspection record concerns Aloe Vera of America, Inc, with an inspection on January 11, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Aloe Vera of America, Inc
Inspection Date
January 11, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · e8786624-c382-406d-8638-8d5da73e2597

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
812882
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

15
  1. 21 CFR 211.166(a)Lack of written stability program
  2. 21 CFR 110.40(a)Precluding contaminants
  3. 21 CFR 111.210(h)(3)(i)Components, verify weight, measure
  4. 21 CFR 111.315(d)Standard reference materials; criteria for selecting
  5. 21 CFR 111.70(b)(3)Specifications - contamination limits
  6. 21 CFR 111.315(b)(3)Sampling plans; finished batches
  7. 21 CFR 111.14(b)(2)Personnel - records - training
  8. 21 CFR 111.325(a)Written procedures, laboratory operations
  9. 21 CFR 111.260(f)Batch record - yield
  10. 21 CFR 111.210(f)Master manufacturing record theoretical and expected yield

Showing 10 of 15 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Aloe Vera of America, Inc

4
DateClassificationOfficeProject area
September 4, 2025NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 2, 2022NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 26, 2018VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 28, 2010NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
Other documents for Aloe Vera of America, Inc
  • FDA Inspection 1280203 - 2025-09-04
  • FDA Inspection 1177724 - 2022-08-02
  • FDA Inspection 1066864 - 2018-09-26
  • FDA Inspection 683997 - 2010-09-28

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