Article 38 The acceptance inspection personnel shall check and verify the appearance, packaging, labeling and qualification documents of the medical devices and make acceptance records, including the name of the medical device, specifications (model), registration certificate number or record certificate number, production batch number or serial number, date of production and validity (or expiration date), Manufacturer, supplier, the number of arrivals, the date of arrival, acceptance of the number of qualified, acceptance results and other content.
Here the qualified documents can be factory inspection reports, just like your raw materials need manufacturers of factory inspection reports, the principle is the same.