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FDA Inspection
•Raca Enterprises, Inc. dba Life Cycle Herbal Products•January 22, 2016

Raca Enterprises, Inc. dba Life Cycle Herbal Products – FDA Inspection, Jan 22, 2016

Record Details

This FDA Inspection record concerns Raca Enterprises, Inc. dba Life Cycle Herbal Products, with an inspection on January 22, 2016, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Raca Enterprises, Inc. dba Life Cycle Herbal Products
Inspection Date
January 22, 2016
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · a72c0da7-0b84-4c90-97f4-bdcfa7580532

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
958333
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ

FDA Citations

8
  1. 21 CFR 111.75(c)(2)Specifications met - test, examinations; compliance
  2. 21 CFR 111.525(a)Returned dietary supplement - specifications
  3. 21 CFR 111.365(h)Mechanical steps - contamination
  4. 21 CFR 111.365Manufacturing operations - prevent contamination
  5. 21 CFR 111.75(c)Specifications met - verify; finished batch
  6. 21 CFR 111.255(b)Batch record - complete
  7. 21 CFR 111.260(j)Batch record - manufacture
  8. 21 CFR 111.105Quality control - ensure quality; package, labeled, master record

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Raca Enterprises, Inc. dba Life Cycle Herbal Products

3
DateClassificationOfficeProject area
December 4, 2014VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 23, 2013OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 20, 2012OAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
Other documents for Raca Enterprises, Inc. dba Life Cycle Herbal Products
  • FDA Inspection 909519 - 2014-12-04
  • FDA Inspection 848592 - 2013-09-23
  • FDA Inspection 794818 - 2012-08-20

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