# FDA Inspection 811110 - Sightlife - December 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/sightlife/34ae8cd2-dd58-4172-805b-5477604dc6fb
Source feed: FDA_Inspections

> FDA Inspection 811110 for Sightlife on December 17, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 811110
- Company Name: Sightlife
- Inspection Date: 2012-12-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d