# Direx Systems Corp. - Inspection Records

Source: https://www.keypedia.com/companies/direx-systems-corp/032cf35f-f13b-4380-8bf7-089beb0314d8

> Inspection records and compliance data for Direx Systems Corp. in Canton, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: Direx Systems Corp.
- FEI Number: 1000513552
- City: Canton
- State: Massachusetts
- Country Name: United States
- Address Line 1: 956 Turnpike St
- Zip Code: 02021

## Related Documents

- [FDA Inspection 1007613 - Direx Systems Corp. - 2017-04-12](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/a53a27a2-f8e9-45c7-a35f-f4fc89c2a0f2) — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2017
- [FDA Inspection 1007613 - Direx Systems Corp. - 2017-04-12](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/46ebc6fb-c47d-47df-9d52-d78aa7c76e22) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 12, 2017
- [FDA Inspection 1007613 - Direx Systems Corp. - 2017-04-12](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/eaac4170-8a4f-4ee0-a185-a0a926d14224) — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2017
- [FDA Inspection 899351 - Direx Systems Corp. - 2014-10-08](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/99bd4d3e-fe7a-4ca9-a8e5-f874d4edc178) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 8, 2014
- [FDA Inspection 899351 - Direx Systems Corp. - 2014-10-08](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/28f333c4-6100-4b01-9fd7-e0507ce1a2b6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 8, 2014
- [FDA Inspection 775404 - Direx Systems Corp. - 2012-04-04](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/8aa9d8c5-cd0b-4f0b-8045-746d6c67491f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2012
- [FDA Inspection 775404 - Direx Systems Corp. - 2012-04-04](https://www.keypedia.com/records/fda_inspections/direx-systems-corp/58e185f4-1bfb-450d-b9a3-0d64975fa3e6) — classification: No Action Indicated (NAI), source: FDA, date: April 4, 2012

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