# Diopsys, Inc. – FDA Inspection, Mar 1, 2010

Source: https://www.keypedia.com/records/fda_inspections/diopsys-inc/57828fd6-e931-4568-bb6e-296787575f3f
Source feed: FDA_Inspections

> FDA inspection 651054 of Diopsys, Inc., March 01, 2010. Classification: Voluntary Action Indicated (VAI). 15 citations under 21 CFR parts 806 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 651054
- Company Name: Diopsys, Inc.
- Inspection Date: 2010-03-01
- 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: 15

## Related Documents

- FDA Inspection 947353 - 2015-11-02
- [FDA Inspection 744141 - 2011-08-11](https://www.keypedia.com/records/fda_inspections/diopsys-inc/a2580df7-19cb-45e6-8457-63f90a107b5b)

Company: https://www.keypedia.com/companies/diopsys-inc/a6eb8d0b-f529-46e2-9151-6446754886be

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