The product was not returned.Product history records were reviewed, and the documentation indicated the product met release criteria.Associated products were not provided.It is unknown, if qualified products were used.The reported lens model is only qualified for use in the company (a) and (b) cartridges.The product investigation could not identify a root cause.According to the patient's self-report, he rubbed his eyes, during the period.And was given symptomatic treatment in time.The manufacturer internal reference number is: (b)(4).
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