FDA Inspection 1302082 - Invibio Device Component Manufacturing, Ltd. (IDCM LTD.) - November 12, 2025

FDA Inspection 1302082 for Invibio Device Component Manufacturing, Ltd. (IDCM LTD.) on November 12, 2025. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1302082 for Invibio Device Component Manufacturing, Ltd. (IDCM LTD.) on November 12, 2025. Classification: No Action Indicated (NAI).

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Record Information

Company

Invibio Device Component Manufacturing, Ltd. (IDCM LTD.)

Inspection Date

November 12, 2025

Product Type

Devices

ID: fa0f719c-7079-4abc-b7d4-344cc4afa8ce

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