# WRP Asia Pacific Sdn Bhd – FDA Inspection, Sep 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/wrp-asia-pacific-sdn-bhd/a1def2da-650c-466d-a43f-ed034fd0208d
Source feed: FDA_Inspections

> FDA inspection 1069387 of WRP Asia Pacific Sdn Bhd, September 27, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069387
- Company Name: WRP Asia Pacific Sdn Bhd
- Inspection Date: 2018-09-27
- 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: 0

## Related Documents

- [FDA Inspection 1136855 - 2019-09-13](https://www.keypedia.com/records/fda_inspections/wrp-asia-pacific-sdn-bhd/65c3b923-323c-449e-b0ac-37e14cfe50d7)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/wrp-asia-pacific-sdn-bhd/e8ac05f9-5e76-4ca6-b2a1-b54b9f62de49

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