San Simeon Inc. in Albuquerque and Chuck’s Seafoods Inc. in Charleston, OR are the latest seafood processors to run into trouble with the Food and Drug Administration over the
Making tuna salad sandwiches or bakery products should not be that hard to understand, but two Maryland businesses are getting some help from the U.S. Food and Drug Administration
Nestle USA and Nestle Heath Care Nutrition each received “Warning Letters” from the U.S. Food and Drug Administration (FDA) earlier this month.
According to the letters, released Tuesday on
The Graham Farm in Moore Haven, FL has a problem with the animal drug sulfamethazine.
Sulfamethazine is an antibacterial drug consisting of any of several synthetic compounds capable of inhibiting
The seafood products at Chaur Fong Inc., include ready-to-eat GIAI PHAT featherback fish “balls,” “cakes,” and “loafs” and cooked seafood products such as HA GAO shrimp dumplings and frozen Featherback
New Hampshire’s Seaport Fish Company is back in the good graces of the U.S. Food & Drug Administration (FDA) after a “Warning Letter” to the Rye, NH-based seafood
Abruzzino’s Italian Bakery, LLC, which sells it products through such retail outlets as Wal-Mart, has not addressed all its food safety problems.
The Food and Drug Administration (FDA) on
Rye, NH-based Seaport Fish Company, LLC offers area restaurants “consistent, high quality fresh and frozen seafood products from around the world.”
The Food and Drug Administration (FDA) inspected Seaport Fish
In every year between 2000 and 2006, and now again in 2009, a Vermont livestock operation has violated federal law by selling cattle for slaughter that had drugs in their
America’s food manufacturers should listen up.
When inspectors from the U.S. Food and Drug Administration (FDA) show up at your facility, these are among things they do not
Tyson Foods Inc. says a Warning Letter it received in November from the U.S. Food & Drug Administration (FDA) made some erroneous conclusions.
“Contrary to the impression left by
Seafood processors came in for their share of “Warning Letters” released Dec. 1st by the U.S. Food and Drug Administration (FDA). The letters, dated from Sept. 23rd to Nov.