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FDA Inspection
•K'An Herb Company, Inc.•July 27, 2016

K'An Herb Company, Inc. – FDA Inspection, Jul 27, 2016

Record Details

This FDA Inspection record concerns K'An Herb Company, Inc., with an inspection on July 27, 2016, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
K'An Herb Company, Inc.
Inspection Date
July 27, 2016
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 076436c2-f227-4338-882b-80e582dc58a5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
986704
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ

FDA Citations

12
  1. 21 CFR 111.27(d)Equipment - maintain, clean, sanitize
  2. 21 CFR 111.15(b)(2)Physical plant - repair
  3. 21 CFR 111.180(b)(3)Documentation - product received; packaging, labeling
  4. 21 CFR 111.20(c)(2)Physical plant - material review and disposition
  5. 21 CFR 111.260(c)Batch record - date, time; maintenance
  6. 21 CFR 111.260(j)(1)Batch record - date, each step
  7. 21 CFR 111.260(j)(2)(ii)Batch record - initials; verifying weight
  8. 21 CFR 111.260(j)(2)(i)Batch record - initials; weighing
  9. 21 CFR 111.260(h)Batch record - results; testing, examination; batch
  10. 21 CFR 111.15(i)Hand-washing facilities

Showing 10 of 12 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of K'An Herb Company, Inc.

3
DateClassificationOfficeProject area
May 23, 2025VAISan Francisco District OfficeFood Composition, Standards, Labeling, and Economics
May 24, 2019VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 27, 2013VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
Other documents for K'An Herb Company, Inc.
  • FDA Inspection 1270850 - 2025-05-23
  • FDA Inspection 1092073 - 2019-05-24
  • FDA Inspection 850625 - 2013-09-27

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