# ActiTech, LP - Inspection Records

Source: https://www.globalkeysolutions.net/companies/actitech-lp/6a6e0ec6-9371-4fe6-88e5-53bdab1f3c8e

> Inspection records and compliance data for ActiTech, LP in Sherman, Texas. Access full analysis and detailed observations.

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## Details

- Name: ActiTech, LP
- FEI Number: 3007005869
- City: Sherman
- State: Texas
- Country Name: United States
- Address Line 1: 301 W Fm 1417
- Zip Code: 75092

## Related Documents

- [FDA Inspection 1105208 - ActiTech, LP - 2019-09-25](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/1b683a93-86d7-4497-8e69-1ae28ae2f11b) — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2019
- [FDA Inspection 749662 - ActiTech, LP - 2011-08-23](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/d7bfdb42-8ed5-4cd9-9d9c-baa491ef2080) — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2011
- [FDA Inspection 749662 - ActiTech, LP - 2011-08-23](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/3cd1dec2-be07-4e5b-a283-011dd124b243) — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2011
- [FDA Inspection 663582 - ActiTech, LP - 2010-05-24](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/3d3e2780-fe3c-4022-99ab-666209264d60) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 24, 2010
- [FDA Inspection 663582 - ActiTech, LP - 2010-05-24](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/628956ea-d5bb-45f1-a865-01707e7ba1b6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 24, 2010
- [FDA Inspection 570526 - ActiTech, LP - 2009-03-13](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/b88212c0-8df4-408b-aefd-7377d0e60618) — classification: No Action Indicated (NAI), source: FDA, date: March 13, 2009
- [FDA Inspection 570526 - ActiTech, LP - 2009-03-13](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/c0f06eca-847b-4a88-be82-39f9f684ed6a) — classification: No Action Indicated (NAI), source: FDA, date: March 13, 2009
- [FDA Inspection 570526 - ActiTech, LP - 2009-03-13](https://www.globalkeysolutions.net/records/fda_inspections/actitech-lp/c3ca5fa8-32eb-41cd-8707-3e298545dcc1) — classification: No Action Indicated (NAI), source: FDA, date: March 13, 2009

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