# FDA Inspection 1099382 - AcuLux, Inc. - August 08, 2019

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

> FDA Inspection 1099382 for AcuLux, Inc. on August 08, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1099382 - 2019-08-08](https://www.keypedia.com/records/fda_inspections/aculux-inc/8ff22b1c-c0b9-47d4-8217-164c4bacd8af)
- [FDA Inspection 940918 - 2015-09-04](https://www.keypedia.com/records/fda_inspections/aculux-inc/7b33c1a1-28d1-4658-900f-bc780d144e04)
- [FDA Inspection 940918 - 2015-09-04](https://www.keypedia.com/records/fda_inspections/aculux-inc/6ad0ac65-19ce-407c-a70e-4292b2ab27f4)
- [FDA Inspection 783891 - 2012-05-30](https://www.keypedia.com/records/fda_inspections/aculux-inc/a74fce64-2d5f-4517-abb9-91134aae38a0)
- [FDA Inspection 783891 - 2012-05-30](https://www.keypedia.com/records/fda_inspections/aculux-inc/9bdf2080-04b2-4a8c-87f6-0e298709ae5a)

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