# FDA Inspection 982423 - Renishaw Mayfield S - July 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/renishaw-mayfield-s/4f4ad75e-405d-458a-9396-4e597e47f1b9
Source feed: FDA_Inspections

> FDA Inspection 982423 for Renishaw Mayfield S on July 21, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982423
- Company Name: Renishaw Mayfield S
- Inspection Date: 2016-07-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/renishaw-mayfield-s/cbcaf74e-a60a-4e62-9cd8-4cf66a79f369

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