From: Center for Food Safety [action@foodsafetynow.org]
Sent: Friday, March 16, 2001 12:05 PM
To: FDA Commissioner
Cc: president@whitehouse.gov; vice.president@whitehouse.gov;
fdadockets@oc.fda.gov; fdadockets@oc.fda.gov
Subject: Oppose the New FDA Regulations on GE Foods!

FDA Commissioner 
Dockets Management Branch (HFA 305)
Food and Drug Administration
5630 Fisher's Lane, rm. 1061
Rockville, MD 20852

RE: Docket No. 00N-1396, and 00D-1598

Dear FDA,
 
I am deeply concerned about your new policies on genetically engineered 
 (GE) foods.
Despite overwhelming consumer demand, your agency still fails to require 
safety testing and mandatory labeling for GE foods. This irresponsibility 
ignores strong scientific evidence of the numerous potential health and 
environmental risks from GE foods. I'm sure you are aware that these foods 
could be toxic, could cause allergic responses, could have lower 
nutritional value, could compromise immune responses in consumers, and 
could cause irreparable damage to the environment. 

I am also greatly opposed to your new “voluntary labeling” policy, which 
potentially denies consumers a basic right to know. Without mandatory 
labeling, it is likely that neither consumers nor health professionals 
will know if an allergic or toxic reaction was the result of a genetically 
engineered food. Consumers will also be deprived of the critical knowledge 
they need to hold food producers responsible should any of these novel 
foods prove hazardous.

Your proposed rules ignore these serious concerns, and appear to be 
decisions based on industry desires and convenience at the expense of 
public health and the environment. I protest your attempt to make me a 
guinea pig of these untested foods! I trust you will take my concern, 
along with the thousands of others, into serious consideration.


Sincerely,



Belynda Saturley
13304 Jefferson Commons
Herndon, VA, 20171

CC: 
The President
Vice President Dick Cheney
FDA Dockets Management [Docket No. 00N-1396]
Senator John W. Warner
Senator George Allen
Representative Frank R. Wolf
Representative Thomas M. Davis, IIIFDA Dockets Management [Docket No. 
00D-1598]


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