The FDA added that its inspectors first found out that the liver spread did not have a CPR after “extensive research” was done in the FDA’s databases.
The LTO, according to the FDA, is “an authorization granted to manufacturers, repackers, importers, distributors, wholesalers, traders who passed FDA guidelines such as Good Manufacturing Practices.” While the company was approved with an LTO, the FDA said that its inspectors also instructed the company to secure CPRs for their products.And why do food products need to be approved by the FDA first before it can be allowed to be sold in the market?
Certification lang pala ang kailangan ng FDA. Pede namang ibatruct ang reno na ihold ang any on going production until masecure ang CPR. Hindi yung ganyan na basta na lang wag daw kakain nito. Engot ampota.
They shouls rebrand their products to 'DITO' so they can skip the long process and have express registration. Even the govt itself will back and lawyer for them if they get into trouble
Hahaha bakit ngayon lang FDA? Wala bang AYUDA ang kumpanya ng RENO sa inyo? Nagtatanong lang...