Analysis for Extraneous Matter

Author:

Dogan Hulya,Subramanyam Bhadriraju

Publisher

Springer International Publishing

Reference82 articles.

1. FDA (2022) Federal Food Drug and Cosmetic Act, as amended. In: Compilation of food and drug laws. Section 201. Authenticated US government information. Accessed from https://www.govinfo.gov/content/pkg/COMPS-973/pdf/COMPS-973.pdf.

2. FDA (2015) Current good manufacturing practice in manufacturing, packing, or holding human food. Part 110, Title 21: food and drugs. In: Code of federal regulations. Office of the Federal Register National Archives and Records Administration, Washington, DC

3. FDA (2018) The food Defect Action Levels - current levels for natural or unavoidable defects for human use that present no health hazard. Department of Health and Human Services, Food and Drug Administration. Washington, DC. Accessed from https://www.fda.gov/food/ingredients-additives-gras-packaging-guidance-documents-regulatory-information/food-defect-levels-handbook

4. FDA (2016) Compliance policy guide manual. Food and Drug Administration, Office of Regulatory Affairs, Washington, DC

5. AOAC International (2016) Extraneous Materials: isolation. In: Official methods of analysis, 20th edn., 2016 (online). AOAC International, Rockville, MD

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