483
The Flex CompanyThe Flex Company – FDA 483, Feb 3, 2023
Record Details
The Flex Company, a medical device manufacturer in Venice, CA, was inspected by the FDA from January 31 to February 3, 2023. The inspection revealed two observations related to inadequate procedures. Specifically, the firm failed to adequately establish procedures for design transfer and for corrective and preventive actions.
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ID · af8a4462-4306-47ce-b34c-70497fbf2edc
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