# FDA Inspection 1297230 - Forefront Medical Technology (Pte) Ltd. - December 18, 2025

Source: https://www.keypedia.com/records/fda_inspections/forefront-medical-technology-pte-ltd/1859e1c9-6d5f-420d-89b2-e63487a1b277
Source feed: FDA_Inspections

> FDA Inspection 1297230 for Forefront Medical Technology (Pte) Ltd. on December 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1297230
- Company Name: Forefront Medical Technology (Pte) Ltd.
- Inspection Date: 2025-12-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1297230 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/forefront-medical-technology-pte-ltd/1b616e49-102b-444d-ba54-0d0407c62608)
- [FDA Inspection 1297230 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/forefront-medical-technology-pte-ltd/91d7289c-423b-4f16-a3f9-da193bb5704b)
- [FDA Inspection 985537 - 2016-07-27](https://www.keypedia.com/records/fda_inspections/forefront-medical-technology-pte-ltd/bed782af-d59d-408e-a675-11a63bd42a81)

Company: https://www.keypedia.com/companies/forefront-medical-technology-pte-ltd/78fcc426-f4b7-4879-bb41-7acf64ddf7fb