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FDA Inspection
•American Natural Products, Inc.•September 20, 2012

American Natural Products, Inc. – FDA Inspection, Sep 20, 2012

Record Details

This FDA Inspection record concerns American Natural Products, Inc., with an inspection on September 20, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
American Natural Products, Inc.
Inspection Date
September 20, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · d9bd1e30-c1f1-4b90-8f27-f6006d93da6e

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
800220
FDA center
Human Drugs
Project area
Unapproved and Misbranded Drugs

FDA Citations

5
  1. 21 CFR 111.65Quality control - quality, dietary supplement
  2. 21 CFR 111.205(a)Master manufacturing record - each batch
  3. 21 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
  4. 21 CFR 111.75(c)(1)Specifications met - verify; production, process control
  5. 21 CFR 111.205(b)(1)Master manufacturing record - specifications; quality

Full citation text and observation details available on the Dashboard.

Other FDA inspections of American Natural Products, Inc.

5
DateClassificationOfficeProject area
July 11, 2025VAIFlorida District OfficeFood Composition, Standards, Labeling, and Economics
May 10, 2022VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 28, 2019VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
October 2, 2017OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
November 8, 2013OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
Other documents for American Natural Products, Inc.
  • FDA Inspection 1275444 - 2025-07-11
  • FDA Inspection 1169053 - 2022-05-10
  • FDA Inspection 1100634 - 2019-08-28
  • FDA Inspection 1027359 - 2017-10-02
  • FDA Inspection 856378 - 2013-11-08

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