Medical device business enterprises should have what record table

In the medical device business equipment acceptance standards have clear provisions, including the first enterprise and the first varieties of approval form (or supplier qualification audit form); purchase records; warehousing acceptance records; warehouse temperature and humidity records, out of the warehouse review records; sales records; unqualified products processing records; after-sales return records; after-sales service records; quality tracking records; user visits, complaints records; medical device adverse event reporting records; transportation records; equipment use and maintenance records; enterprise staff training records; medical device process records and documents; fitting, review records; fitting enterprises disinfecting Event report records; transportation records; equipment use and maintenance records; employee training records; medical device process records and vouchers filed records; fitting, review records; disinfection records of the fitting enterprise; system implementation inspection and assessment records

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