FDA Inspection 1302082 — Invibio Device Component Manufacturing, Ltd. (IDCM LTD.)
The FDA completed an inspection of Invibio Device Component Manufacturing, Ltd. (IDCM LTD.) on November 12, 2025 in Thornton-Cleveleys. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 12, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Thornton-Cleveleys (United Kingdom)