# FDA Inspection 1321566 - Hi Tech Mold & Tool, Inc. - June 11, 2026

Source: https://www.keypedia.com/records/fda_inspections/hi-tech-mold-tool-inc/196b166b-f8e5-4203-b916-79bc50b4645b
Source feed: FDA_Inspections

> FDA Inspection 1321566 for Hi Tech Mold & Tool, Inc. on June 11, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1321566
- Company Name: Hi Tech Mold & Tool, Inc.
- Inspection Date: 2026-06-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1321566 - 2026-06-11](https://www.keypedia.com/records/fda_inspections/hi-tech-mold-tool-inc/c927cf53-fa13-4501-a89d-e966c08d701d)
- [FDA Inspection 888858 - 2014-07-30](https://www.keypedia.com/records/fda_inspections/hi-tech-mold-tool-inc/d2b41173-e22a-4f46-af80-1717ba2e5dab)

Company: https://www.keypedia.com/companies/hi-tech-mold-tool-inc/37895959-341f-4ec8-8b30-d8bd2c307533

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7