# Renishaw Mayfield S – FDA Inspection, Jul 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/renishaw-mayfield-s/ca336692-5d9b-4d35-8129-53f8d2ce628a
Source feed: FDA_Inspections

> FDA inspection 982423 of Renishaw Mayfield S, July 21, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation 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: 982423
- Company Name: Renishaw Mayfield S
- Inspection Date: 2016-07-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1275706 - 2025-06-12](https://www.keypedia.com/records/fda_inspections/renishaw-mayfield-s/cf7591f6-e7c0-42ea-82e2-60b37600989a)

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