# HFX, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/hfx-inc/1254f459-ae1d-4b62-9e70-19f7009aec80

> Inspection records and compliance data for HFX, Inc. in Claysburg, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: HFX, Inc.
- FEI Number: 3005051863
- City: Claysburg
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 12985 Dunnings Hwy
- Zip Code: 16625

## Related Documents

- [FDA Inspection 1106429 - HFX, Inc. - 2019-09-10](https://www.globalkeysolutions.net/records/fda_inspections/hfx-inc/f6dd0f60-3f34-42b6-b674-fd687677db7e) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2019
- [FDA Inspection 1106429 - HFX, Inc. - 2019-09-10](https://www.globalkeysolutions.net/records/fda_inspections/hfx-inc/6cefabde-b40a-4b83-b534-82cf7a836b6b) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2019
- [FDA Inspection 961498 - HFX, Inc. - 2016-01-11](https://www.globalkeysolutions.net/records/fda_inspections/hfx-inc/6939570e-6a14-4ceb-88e6-85505e7687e1) — classification: No Action Indicated (NAI), source: FDA, date: January 11, 2016
- [FDA Inspection 817508 - HFX, Inc. - 2013-01-30](https://www.globalkeysolutions.net/records/fda_inspections/hfx-inc/aa2373fd-da4f-4ca3-890c-730fe98bfbc7) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2013
- [FDA Inspection 817508 - HFX, Inc. - 2013-01-30](https://www.globalkeysolutions.net/records/fda_inspections/hfx-inc/0e6ac0f3-6ccb-4271-96f1-f4fca1fa7c03) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2013
- [FDA Inspection 677194 - HFX, Inc. - 2010-08-20](https://www.globalkeysolutions.net/records/fda_inspections/hfx-inc/c541e613-38e1-4b7f-b3e8-1fa3678ec112) — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2010
- [FDA Inspection 598337 - HFX, Inc. - 2009-07-02](https://www.globalkeysolutions.net/records/fda_inspections/hfx-inc/ae2ca2e8-63bf-41f8-a4f2-2d2bac2c4480) — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2009

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