# FDA Inspection 1222582 - Nulatex Sdn. Bhd. - October 19, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/nulatex-sdn-bhd/bb4e1ff3-fac9-4d24-be58-0aba1c09990e
Source feed: FDA_Inspections

> FDA Inspection 1222582 for Nulatex Sdn. Bhd. on October 19, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1222582
- Company Name: Nulatex Sdn. Bhd.
- Inspection Date: 2023-10-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 945942 - 2015-09-10](https://www.globalkeysolutions.net/records/fda_inspections/nulatex-sdn-bhd/d22f0b83-beab-455e-a05d-3099db33a270)
- [FDA Inspection 945942 - 2015-09-10](https://www.globalkeysolutions.net/records/fda_inspections/nulatex-sdn-bhd/895ab5ce-e65f-41d7-8728-fe7dc705ec67)

Company: https://www.globalkeysolutions.net/companies/nulatex-sdn-bhd/a3cd42f6-0389-4380-bcb6-db79f0eef681

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