# Phoenix Diagnostics, Inc., Natick, MA – FDA Inspections

Source: https://www.keypedia.com/companies/phoenix-diagnostics-inc/e6758401-487c-47a5-8942-ac7f5e87b05a

> Inspection records and compliance data for Phoenix Diagnostics, Inc. in Natick, Massachusetts. 4 FDA inspections on record, 1 Form 483, last inspected March 17, 2022.

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## Details

- Name: Phoenix Diagnostics, Inc.
- FEI Number: 1222035
- Address Line 1: 8 Tech Cir
- City: Natick
- State: Massachusetts
- Zip Code: 01760
- Country Name: United States
- Address: 8 Tech Cir, Natick, Massachusetts 01760, United States
- Country: United States

## Related Documents

- [483 - Phoenix Diagnostics, Inc. - 2022-03-17](https://www.keypedia.com/records/483/phoenix-diagnostics-inc/93e2af9e-e533-4618-83f9-f8a0915518f7) — source: FDA, date: March 17, 2022
- FDA Inspection 1164713 - Phoenix Diagnostics, Inc. - 2022-03-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 17, 2022
- FDA Inspection 1164713 - Phoenix Diagnostics, Inc. - 2022-03-17 — classification: No Action Indicated (NAI), source: FDA, date: March 17, 2022
- [FDA Inspection 1022108 - Phoenix Diagnostics, Inc. - 2017-08-18](https://www.keypedia.com/records/fda_inspections/phoenix-diagnostics-inc/fd34080b-275f-46d4-9da2-a471a13af3b6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 18, 2017
- FDA Inspection 1022108 - Phoenix Diagnostics, Inc. - 2017-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2017
- [FDA Inspection 792557 - Phoenix Diagnostics, Inc. - 2012-07-26](https://www.keypedia.com/records/fda_inspections/phoenix-diagnostics-inc/dacd52aa-c5f5-4638-bb09-78dadfdc6e09) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 26, 2012
- FDA Inspection 602295 - Phoenix Diagnostics, Inc. - 2009-08-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 6, 2009
- FDA Inspection 602295 - Phoenix Diagnostics, Inc. - 2009-08-06 — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2009

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