# Sightlife, Seattle, WA – FDA Inspections

Source: https://www.keypedia.com/companies/sightlife/7bfeee4c-fe3f-4f4d-8837-5845b36d913c

> Inspection records and compliance data for Sightlife in Seattle, Washington. 8 FDA inspections on record, 1 Form 483, last inspected April 30, 2026.

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## Details

- Name: Sightlife
- FEI Number: 3001239136
- Address Line 1: 1200 6th Ave Ste 300
- City: Seattle
- State: Washington
- Zip Code: 98101
- Country Name: United States
- Address: 1200 6th Ave Ste 300, Seattle, Washington 98101, United States
- Country: United States

## Related Documents

- FDA Inspection 1318978 - Sightlife - 2026-04-30 — source: FDA, date: April 30, 2026
- FDA Inspection 1254770 - Sightlife - 2024-11-18 — source: FDA, date: November 18, 2024
- FDA Inspection 1254770 - Sightlife - 2024-11-18 — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2024
- FDA Inspection 1198187 - Sightlife - 2023-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2023
- FDA Inspection 1198187 - Sightlife - 2023-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2023
- FDA Inspection 1198187 - Sightlife - 2023-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2023
- [EIR - Sightlife - 2017-10-13](https://www.keypedia.com/records/eir/sightlife/ba7e4a40-b463-4453-be4a-12a690715323) — source: FDA, date: October 13, 2017
- [FDA Inspection 1028861 - Sightlife - 2017-10-13](https://www.keypedia.com/records/fda_inspections/sightlife/b7c48c7a-0299-4259-84d9-154fc5f94dd2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 13, 2017
- FDA Inspection 1028861 - Sightlife - 2017-10-13 — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2017
- [FDA Inspection 963070 - Sightlife - 2016-03-14](https://www.keypedia.com/records/fda_inspections/sightlife/d14e380d-3687-41e2-a386-46cfee6b16d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2016
- FDA Inspection 855215 - Sightlife - 2013-11-14 — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2013

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