# VisionGift - Inspection Records

Source: https://www.keypedia.com/companies/visiongift/f6572d7f-64b9-47a2-b217-a5453d1eb4e5

> Inspection records and compliance data for VisionGift in Portland, Oregon. Access full analysis and detailed observations.

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## Details

- Name: VisionGift
- FEI Number: 3001239138
- City: Portland
- State: Oregon
- Country Name: United States
- Address Line 1: 2201 Se 11th Ave
- Zip Code: 97214

## Related Documents

- [FDA Inspection 1225569 - VisionGift - 2023-12-04](https://www.keypedia.com/records/fda_inspections/visiongift/38f9a83b-4342-47a1-9f7d-9f22574aa4d1) — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2023
- [FDA Inspection 1225569 - VisionGift - 2023-12-04](https://www.keypedia.com/records/fda_inspections/visiongift/9aad0161-5497-4e13-b82f-47272c959f9a) — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2023
- [FDA Inspection 1102889 - VisionGift - 2019-09-25](https://www.keypedia.com/records/fda_inspections/visiongift/73a84fd1-3509-4c78-bab9-c0f828a0d04a) — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2019
- [FDA Inspection 968164 - VisionGift - 2016-04-29](https://www.keypedia.com/records/fda_inspections/visiongift/7d953743-4342-4d22-8793-203e001101f1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 29, 2016
- [FDA Inspection 895861 - VisionGift - 2014-09-18](https://www.keypedia.com/records/fda_inspections/visiongift/312787d7-4068-4690-aa01-929e83545897) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2014
- [FDA Inspection 756331 - VisionGift - 2011-12-02](https://www.keypedia.com/records/fda_inspections/visiongift/6ac2de89-a367-4a2a-8bcd-87f1cfec8083) — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2011
- [FDA Inspection 667066 - VisionGift - 2010-06-16](https://www.keypedia.com/records/fda_inspections/visiongift/5f921d17-d419-4e18-8a57-5bb847749d75) — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2010

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