# Bioforce USA - Inspection Records

Source: https://www.globalkeysolutions.net/companies/bioforce-usa/fef435e0-0c9e-45d0-b233-340d45ac56ba

> Inspection records and compliance data for Bioforce USA in Ghent, New York. Access full analysis and detailed observations.

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## Details

- Name: Bioforce USA
- FEI Number: 3006152755
- City: Ghent
- State: New York
- Country Name: United States
- Address Line 1: 6 Grandinetti Dr
- Zip Code: 12075

## Related Documents

- [FDA Inspection 1269368 - Bioforce USA - 2025-05-08](https://www.globalkeysolutions.net/records/fda_inspections/bioforce-usa/ed0f9461-0512-4d2b-ae4c-c5922d851f8f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 8, 2025
- [FDA Inspection 1261415 - Bioforce USA - 2025-02-12](https://www.globalkeysolutions.net/records/fda_inspections/bioforce-usa/b4b4712c-a4fa-415f-a6db-2b802343723f) — source: FDA, date: February 12, 2025
- [FDA Inspection 1261415 - Bioforce USA - 2025-02-12](https://www.globalkeysolutions.net/records/fda_inspections/bioforce-usa/83a6f27c-4131-49cd-9e39-ffec6ebd94ea) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2025
- [FDA Inspection 1064687 - Bioforce USA - 2018-08-29](https://www.globalkeysolutions.net/records/fda_inspections/bioforce-usa/15ea0e52-0e72-431d-9903-94ce39c32fe0) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2018
- [FDA Inspection 1064687 - Bioforce USA - 2018-08-29](https://www.globalkeysolutions.net/records/fda_inspections/bioforce-usa/48fb2dea-c1d8-472a-bd1b-f3819045fae7) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2018
- [FDA Inspection 745314 - Bioforce USA - 2011-09-19](https://www.globalkeysolutions.net/records/fda_inspections/bioforce-usa/0e131577-0a3e-462c-a288-64915decf669) — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2011
- [FDA Inspection 745314 - Bioforce USA - 2011-09-19](https://www.globalkeysolutions.net/records/fda_inspections/bioforce-usa/afa637bc-37c1-41d0-9d40-a7940bb0dd2f) — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2011

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