For Immediate Release: February 1, 2013Media Inquiries: Pat El-Hinnawy, 301-796-4763, patricia.el-hinnawy@fda.hhs.govConsumer Inquiries: 888-INFO-FDA Michigan soy processor is under court order to meet FDA food safety standardsMultiple inspections found manufacturing violations and insanitary conditions Green Hope LLC, which does business as Rosewood Products, and owner, Phi G. Ye, of Ann Arbor, Mich., have agreed to a…
Posts Tagged ‘ Federal Food ’
Federal judge approves consent decree with Ben Venue Laboratories
FDA NEWS RELEASE For Immediate Release: Jan. 31, 2013Media Inquiries: Sarah Clark-Lynn, 301-796-9110, sarah.clark-lynn@fda.hhs.gov Consumer Inquiries: 888-INFO-FDA Federal judge approves consent decree with Ben Venue Laboratories Company repeatedly failed to comply with good manufacturing practices prompting action The U.S. Food and Drug Administration announced today that a federal judge has approved a consent decree of…
FDA: Puerto Rico beverage manufacturer enters into consent decree
FDA NEWS RELEASE For Immediate Release: Jan. 25, 2013 Media Inquiries: Tamara Ward, 301-796-7567, tamara.ward@fda.hhs.govConsumer Inquiries: 888-INFO-FDA En Español FDA: Puerto Rico beverage manufacturer enters into consent decreeDefendants will stop distributing adulterated products with false claims The U.S. Food and Drug Administration announced today that Jonlly Fruits, Inc. (Jonlly), and its President, Bartolo Pérez Román…
Judge Rules Plaintiffs’ Experts May Sample and Test NECC Facility for…
- We devise to be in there a full 4 days, nonetheless a experts should be means to establish a lot from a rough sweep. Boston, MA (PRWEB) Dec 10, 2012 A judge ruled Dec.10 that experts hired by victims of a meningitis conflict related to a New England Compounding Center might enter a trickery…
Updated FDA Statement on Compounded Versions of hydroxyprogesterone caproate (the active ingredient in Makena)
For Immediate Release: June 15, 2012Media Inquiries: Erica Jefferson, 301-796-4988, Erica.Jefferson@fda.hhs.gov Updated FDA Statement on Compounded Versions of hydroxyprogesterone caproate (the active ingredient in Makena) FDA (or the Agency) approved Makena (hydroxyprogesterone caproate) in February 2011 for the reduction of the risk of certain preterm births in women who have had at least one prior…
U.S. Marshals seize unapproved and misbranded drug products at Missouri distributor
For Immediate Release: March 29, 2012Media Inquiries: FDA: Pat El-Hinnawy, 301-796-4763, patricia.el-hinnawy@fda.hhs.gov; U.S. Attorney’s Office: Don Ledford, 816-426-4220, Don.Ledford@usdoj.govConsumer Inquiries: 888-INFO-FDA U.S. Marshals seize unapproved and misbranded drug products at Missouri distributor Dara Corrigan, associate commissioner for regulatory affairs for the U.S. Food and Drug Administration, and David M. Ketchmark, Acting U.S. Attorney for the Western…
Follow us
