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» Filings of Food Additive Petitions: Ajinomoto Co., Inc.; Amendment
Filings of Food Additive Petitions: Ajinomoto Co., Inc.; Amendment
Document ID:
FDA-2009-F-0303-0004
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2012-26315
CFR Citation:
21 CFR Part 172
View Document:
Details Information
Document Subtype:
General Notice
Received Date:
October 26 2012, at 12:00 AM Eastern Daylight Time
Start-End Page:
65340 - 65341
Page Count:
2
Comment Start Date:
October 26 2012, at 12:00 AM Eastern Standard Time
Comment Due Date:
November 26 2012, at 11:59 PM Eastern Standard Time
Comments
Total:
1
Sam James Scheurich - Comment
Posted:
11/02/2012
ID:
FDA-2009-F-0303-0005
Comment Period Closed
Nov 26,2012 11:59 PM ET
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Total:
12
Filings of Food Additive Petitions: Ajinomoto Co., Inc.; Amendment
Filing of Amendment to Food Additive Petition: Nexira
Filing of Amendment to Food Additive Petition: Nexira
Food Additives Permitted for Direct Addition to Food for Human Consumption: Vitamin D2 Bakers Yeast
Gruma Corp., Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza; Filings of Food Additive Petition; Correction
Gruma Corporation, Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza; Filing of Food Additive Petition
Filings of Food Additive Petitions: Abbott Laboratories
Filings of Food Additive Petitions: Nexira
Food Additives Permitted for Human Consumption: Hydroxypropyl Cellulose
Food Additives Permitted for Direct Addition to Food for Human Consumption: Bacteriophage Preparation
Food Additives Permitted for Direct Addition to Food for Human Consumption: Silver Nitrate and Hydrogen Peroxide
Food Additives Permitted for Direct Addition to Food for Human Consumption: Vitamin D
Filings of Food Additive Petitions: Ajinomoto Co., Inc.; Amendment
Details Information
Comments
Posted: 11/02/2012 ID: FDA-2009-F-0303-0005
Nov 26,2012 11:59 PM ET
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