# AcuFocus, Inc. – FDA Inspection, Jan 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/acufocus-inc/92e2e212-5a2f-4d51-97f6-5938f4556cb6
Source feed: FDA_Inspections

> FDA inspection 815296 of AcuFocus, Inc., January 18, 2013. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 815296
- Company Name: AcuFocus, Inc.
- Inspection Date: 2013-01-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 980730 - 2016-06-24

Company: https://www.keypedia.com/companies/acufocus-inc/ec930090-d605-4d4b-a185-64b5a86f7577

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7