# WARDRAY PREMISE LTD – FDA Inspection, Oct 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/wardray-premise-ltd/daae5f29-353d-42a9-bcf0-f26ed1b90a57
Source feed: FDA_Inspections

> FDA inspection 1030855 of WARDRAY PREMISE LTD, October 13, 2017. 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: 1030855
- Company Name: WARDRAY PREMISE LTD
- Inspection Date: 2017-10-13
- 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 1261293 - 2025-01-09](https://www.keypedia.com/records/fda_inspections/wardray-premise-ltd/c2992da0-0bed-45b1-89fd-2fa8e4310fe8)

## Related Officers

- [Investigator](https://www.keypedia.com/people/akbar-j-zaidi/9cd9ac91-2d4b-4f6f-a975-865342075924)

Company: https://www.keypedia.com/companies/wardray-premise-ltd/1a979f53-2461-4dcb-999e-d4f9f93737a5

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