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4 Nov 2009, 2:00 pm
Any adverse events that may be related to the use of the Recalled Products should be reported to the FDA's MedWatch Adverse Event Reporting program online [at www.fda.gov/MedWatch/report.htm], by phone [1-800-FDA-1088], or by returning the postagepaid FDA form 3500 [which may be downloaded from www.fda.gov/MedWatch/getforms.htm] by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA- 0178]. [read post]
17 Sep 2007, 10:14 pm
Gissel Packing Co., 395 U.S. 575, at 618 (1969), the Board agreed with the judge's finding of violation of Section 8(a)(1). [read post]