# Innolatex Sdn. Bhd. – FDA Inspection, Jul 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/innolatex-sdn-bhd/7404a2f6-8a69-4b69-8bf4-d269c82a9439
Source feed: FDA_Inspections

> FDA inspection 1215638 of Innolatex Sdn. Bhd., July 27, 2023. Classification: Voluntary Action Indicated (VAI). 8 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: 1215638
- Company Name: Innolatex Sdn. Bhd.
- Inspection Date: 2023-07-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- FDA Inspection 1009128 - 2017-03-09
- FDA Inspection 752824 - 2011-11-03
- [FDA Inspection 709156 - 2011-01-20](https://www.keypedia.com/records/fda_inspections/innolatex-sdn-bhd/a810433c-b08b-44c3-89a5-e10705837ce8)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brittani-n-franklin/1d5e9344-1145-42ff-a175-5541b565b15e)

Company: https://www.keypedia.com/companies/innolatex-sdn-bhd/f67b8a34-aa42-434f-b1b6-c83e2fbe9c98

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