483
Kurin, Inc.Kurin, Inc. – FDA 483, Jan 9, 2026
Record Details
Kurin, Inc. in San Diego, CA, was inspected regarding its manufacturing operations. The inspection revealed significant deficiencies in the firm's complaint handling procedures, specifically concerning the documentation of Medical Device Report (MDR) related complaint investigations. These issues included incomplete product and contact information, and inadequate documentation of corrective actions.
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ID · 8f010c54-ba0f-43fb-bbf8-d86b949182e2
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