# AcuLux, Inc. – FDA Inspection, Aug 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/aculux-inc/afc0ab4c-518d-4e61-9cd9-e9f2645ca749
Source feed: FDA_Inspections

> FDA inspection 1099382 of AcuLux, Inc., August 08, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099382
- Company Name: AcuLux, Inc.
- Inspection Date: 2019-08-08
- 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: 2

## Related Documents

- [FDA Inspection 940918 - 2015-09-04](https://www.keypedia.com/records/fda_inspections/aculux-inc/7b33c1a1-28d1-4658-900f-bc780d144e04)
- [FDA Inspection 783891 - 2012-05-30](https://www.keypedia.com/records/fda_inspections/aculux-inc/a74fce64-2d5f-4517-abb9-91134aae38a0)
- FDA Inspection 598305 - 2009-02-25

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stanley-b-eugene/4708f43e-0592-4c24-b276-d9f9092788a3)

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