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FDA Inspection
•Xymogen Manufacturing, LLC•August 16, 2018

Xymogen Manufacturing, LLC – FDA Inspection, Aug 16, 2018

Record Details

This FDA Inspection record concerns Xymogen Manufacturing, LLC, with an inspection on August 16, 2018, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Xymogen Manufacturing, LLC
Inspection Date
August 16, 2018
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
People
  • Lizaida E. Rodriguez (Issuing Officer)
  • Sandra Carpio (Issuing Officer)
View Company Profile

ID · ef883075-81f1-4201-b9a8-a26fffcb6b70

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1062310
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 111.570(b)(2)(ii)(F)Record - product complaint; findings
  2. 21 CFR 111.73Specifications met - quality
  3. 21 CFR 111.415(b)Dietary supplement - protect, contamination

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Xymogen Manufacturing, LLC

6
DateClassificationOfficeProject area
August 13, 2024VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 8, 2022NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 10, 2014VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
May 24, 2013OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
July 6, 2012VAICenter for Drug Evaluation and ResearchUnapproved and Misbranded Drugs
View all 6 other inspections on the company page
Other documents for Xymogen Manufacturing, LLC
  • FDA Inspection 1246381 - 2024-08-13
  • FDA Inspection 1181480 - 2022-08-08
  • FDA Inspection 897690 - 2014-09-10
  • FDA Inspection 833513 - 2013-05-24
  • FDA Inspection 790122 - 2012-07-06

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