What is CE and FDA

All the disposable face masks (mouth masks), KN95 medical face masks, Disposable Medical Protective clothing & Suits Medical Safety ApparelMedical Safety Glasses & lab Goggles, 2019-nCov 2019-Novel Coronavirus test kit & vaccine (later), Medical tympanic and forehead Digital thermometers, infrared surface thermometer and other Medical equitments maskbus  we sell all available with CE certification. NO FDA

What is CE certification? -- Maskbus.com

CE marking is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA).The CE marking is also found on products sold outside the EEA that have been manufactured to EEA standards. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. It is in that sense similar to the FCC Declaration of Conformity used on certain electronic devices sold in the United States. The CE marking is the manufacturer's declaration that the product meets EU standards for health, safety, and environmental protection. The mark consists of the CE logo and, if applicable, the four digit identification number of the Notified Body involved in the conformity assessment procedure. "CE" is sometimes indicated as an abbreviation of "Conformité Européenne" (French for "European Conformity"), but is not defined as such in the relevant legislation. The CE mark indicates that the product may be sold freely in any part the European Economic Area, irrespective of its country of origin. 

What Is the FDA ( Food and Drug Administration )? - Maskbus.com

The Food and Drug Administration (FDA) is a government agency established in 1906 with the passage of the Federal Food and Drugs Act. The agency is separated into divisions that oversee a majority of the organization's obligations involving food, drugs, cosmetics, animal food, dietary supplements, medical devices, biological goods, and blood products.
 
Understanding the Food and Drug Administration (FDA)
The FDA is known for its work in regulating the development of new drugs. The FDA has developed rules regarding the clinical trials that must be done on all new medications. Pharmaceutical companies must test drugs through four phases of clinical trials before they can be marketed to individuals.
 
The FDA is relevant for investors specifically in regards to biotech and pharmaceutical companies. FDA approval can be crucial to companies that are heavily involved in developing new drugs. Without the agency’s approval, regulated products under the FDA's purview cannot be released for sale in the United States.