# FDA Inspection 975498 - Pleasure Latex Products SDN BHD - April 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/pleasure-latex-products-sdn-bhd/283fff9e-d876-4149-87ca-3f35e4a215bc
Source feed: FDA_Inspections

> FDA Inspection 975498 for Pleasure Latex Products SDN BHD on April 28, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 975498
- Company Name: Pleasure Latex Products SDN BHD
- Inspection Date: 2016-04-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1180886 - 2022-09-08](https://www.keypedia.com/records/fda_inspections/pleasure-latex-products-sdn-bhd/f6a00578-5708-4a7d-a298-5534644677c3)

Company: https://www.keypedia.com/companies/pleasure-latex-products-sdn-bhd/41a5d89b-bf9e-46fb-9f3c-6b1912746272

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