# Pleasure Latex Products SDN BHD – FDA Inspection, Apr 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 of Pleasure Latex Products SDN BHD, April 28, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- 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: 5

## Related Documents

- FDA Inspection 1180886 - 2022-09-08

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
