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Specifically, the FDA is being taken to task for:
Requiring products released after February 15, 2007 to be verified by the FDA before going on sale
Taxing cigar and pipe companies with user fees, which could add up to $65 million a year
Violating the Regulatory Flexibility Act by neglecting to assess the effects of the Final Rule on small businesses
Requiring cigar health warning labels to take up 30% of a package?s display panels
Pigeon-holing companies who blend finished pipe tobacco or create cigar samplers of finished cigars as "manufacturers,? which means they?ll face stricter regulations than ?retailers?
The president of the Cigar Association of America, Craig Williamson, said of the decision to file suit: "We hoped the FDA would craft a flexible regulatory structure that accounted for the uniqueness of our industry. Instead, we got a broad, one-size-fits-all rule that fails to account for how cigars and premium cigars are manufactured, distributed, sold and consumed in the United States."
So what happens if the Final Rule really is final? Cigar companies will have a two year window to sell their current inventory before the new regulations kick in. After that, there?s no telling what the business will look like.