# AcuLux, Inc. – FDA Inspection, May 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/aculux-inc/a74fce64-2d5f-4517-abb9-91134aae38a0
Source feed: FDA_Inspections

> FDA inspection 783891 of AcuLux, Inc., May 30, 2012. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 783891
- Company Name: AcuLux, Inc.
- Inspection Date: 2012-05-30
- 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: 7

## Related Documents

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- [FDA Inspection 940918 - 2015-09-04](https://www.keypedia.com/records/fda_inspections/aculux-inc/7b33c1a1-28d1-4658-900f-bc780d144e04)
- FDA Inspection 598305 - 2009-02-25

Company: https://www.keypedia.com/companies/aculux-inc/1f996d0f-92a6-4e95-ba7f-4f2cc71ce6ec

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