# Hyperbaric Technologies Inc., Amsterdam, NY – FDA Inspections

Source: https://www.keypedia.com/companies/hyperbaric-technologies-inc/1047fd88-b5b6-4a3c-b7e9-6a61962330ba

> Inspection records and compliance data for Hyperbaric Technologies Inc. in Amsterdam, New York. 4 FDA inspections on record, 1 Form 483, last inspected September 26, 2018.

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## Details

- Name: Hyperbaric Technologies Inc.
- FEI Number: 1000624398
- Address Line 1: 1 Sam Stratton Rd
- City: Amsterdam
- State: New York
- Zip Code: 12010
- Country Name: United States
- Address: 1 Sam Stratton Rd, Amsterdam, New York 12010, United States
- Country: United States

## Related Documents

- [FDA Inspection 1066879 - Hyperbaric Technologies Inc. - 2018-09-26](https://www.keypedia.com/records/fda_inspections/hyperbaric-technologies-inc/e1ab615f-9f96-4eff-a7ae-eec03f5d3844) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 26, 2018
- FDA Inspection 1066879 - Hyperbaric Technologies Inc. - 2018-09-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 26, 2018
- FDA Inspection 819582 - Hyperbaric Technologies Inc. - 2013-02-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 20, 2013
- FDA Inspection 819582 - Hyperbaric Technologies Inc. - 2013-02-20 — classification: No Action Indicated (NAI), source: FDA, date: February 20, 2013
- FDA Inspection 709392 - Hyperbaric Technologies Inc. - 2011-02-04 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 4, 2011
- FDA Inspection 709392 - Hyperbaric Technologies Inc. - 2011-02-04 — classification: No Action Indicated (NAI), source: FDA, date: February 4, 2011
- FDA Inspection 578886 - Hyperbaric Technologies Inc. - 2009-05-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2009
- [FDA Inspection 578886 - Hyperbaric Technologies Inc. - 2009-05-12](https://www.keypedia.com/records/fda_inspections/hyperbaric-technologies-inc/b551cba2-4118-4ece-bdb5-6702e67f52d3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2009

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