Barcelona Nut Company Recalls Roasted and Salted in Shell …
Barcelona Nut Company of Baltimore, Maryland is recalling 239 cases of roasted and salted in shell pistachios, because it has the potential to be contaminated with Salmonella, an organism that...
Manufacturing Facilities | Grifols Partnership Parenteral CDMO
Grifols operates two FDA and GMP approved manufacturing facilities in Spain (Barcelona and Murcia) capable of handling pharmaceutical products and medical devices with various technological capabilities.
Produce Packaging, Inc. Recalls Red Curry Grain Bowl and Barcelona ...
Produce Packaging, Inc. of Willoughby Hills, OH is voluntarily recalling its Red Curry Grain Bowl and Barcelona Vinaigrette Grain Bowl. These are being recalled because they contain an undeclared...
Proandre SL - 567234 - 02/13/2019 | FDA
The U.S. Food and Drug Administration (FDA) inspected your drug manufacturing facility, Proandre SL at Calle Condestable De Portugal 43-45, Granollers, Barcelona, from June 11 to 14, 2018. This...
www.fda.gov IMPLANT PROTESIS DENTAL 2004, S.l. Francesc Fumanal Regulatory Affairs Manager Carrer Rosa dels Vents, 9-15. Premià de Dalt (Barcelona), 08338 SPAIN Re: K242819 Trade/Device Name: IPD Dental Implant Abutments Regulation Number: 21 CFR 872.3630 Regulation Name: Endosseous Dental Implant Abutment Regulatory Class: Class II
Grifols demana llicència a la FDA dels Estats Units per al seu nou ...
Jan 9, 2025 · La farmacèutica catalana especialitzada en plasma sanguini Grifols ha anunciat aquest dijous que ha presentat sol·licitud davant la FDA dels Estats Units per rebre la llicència del seu nou producte, un fibrinogen que va ser presentat a Europa l'octubre de l'any passat. L'anunci coincideix just amb el dia en què l'empresa compleix un any des dels atacs rebuts pel fons baixista Gotham ...
www.fda.gov December 6, 2024 Ames Medical Prosthetic Solutions, S.A.U. Emili Tarrats Plant Director Ctra. Laurea Miro 388 Sant Feliu de Llobregat, Barcelona 08980 Spain Re: K240461 ... 08620 Sant Vicenç dels Horts, Barcelona SPAIN CONTACT: Emili …
deepull receives FDA Breakthrough Device Designation for its …
Dec 5, 2024 · deepull, a medical device company developing culture-free diagnostic solutions for rapid pathogen identification, announced today that it has received Breakthrough Device Designation from the U.S. Food and Drug Administration (FDA) for its UllCORE Bloodstream Infection (BSI) Test.
La FDA autoriza la comercialización de 20 productos de bolsa de ...
1 day ago · Los productos para los que la FDA ha emitido órdenes de autorización de comercialización son los siguientes, cada uno con dos concentraciones de nicotina (3 miligramos y 6 miligramos): ZYN ...
Kerstin Noëlle Vokinger: ‘New cancer therapies are being …
Sep 21, 2024 · So, we wanted to investigate whether the approval of new therapies by organizations such as the European Medicines Agency [EMA] or the United States agency [FDA] is aligned with clinical trials.