# VueTek Scientific, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vuetek-scientific-llc/ea40b489-442c-455b-b528-85b7d893dea5

> Inspection records and compliance data for VueTek Scientific, LLC in Gray, Maine. Access full analysis and detailed observations.

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## Details

- Name: VueTek Scientific, LLC
- FEI Number: 3009170195
- City: Gray
- State: Maine
- Country Name: United States
- Address Line 1: 22 Shaker Rd
- Zip Code: 04039

## Related Documents

- [FDA Inspection 1101010 - VueTek Scientific, LLC - 2019-08-21](https://www.globalkeysolutions.net/records/fda_inspections/vuetek-scientific-llc/549a3bb0-6cf4-468e-b900-5279ed22e223) — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2019
- [FDA Inspection 1101010 - VueTek Scientific, LLC - 2019-08-21](https://www.globalkeysolutions.net/records/fda_inspections/vuetek-scientific-llc/625aa9cc-5455-4cd6-92d9-786a33d54b7a) — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2019
- [FDA Inspection 817848 - VueTek Scientific, LLC - 2013-01-24](https://www.globalkeysolutions.net/records/fda_inspections/vuetek-scientific-llc/6a57aaa8-d34d-49cb-a1b2-58d9e0979232) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2013
- [FDA Inspection 817848 - VueTek Scientific, LLC - 2013-01-24](https://www.globalkeysolutions.net/records/fda_inspections/vuetek-scientific-llc/dea4853b-37f5-4ac8-b0ed-ace2abe3bb57) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2013
- [FDA Inspection 702420 - VueTek Scientific, LLC - 2010-12-17](https://www.globalkeysolutions.net/records/fda_inspections/vuetek-scientific-llc/eb503fa1-ab57-495f-8d8a-472ebe4d737a) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2010
- [FDA Inspection 702420 - VueTek Scientific, LLC - 2010-12-17](https://www.globalkeysolutions.net/records/fda_inspections/vuetek-scientific-llc/fb1f4adf-2d9a-4ea1-8ab3-b5b4a2a40bab) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2010

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