# FDA Inspection 1026856 - Renner & Co - September 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/renner-co/e0a7c4cf-b7ab-4997-b28c-66cb58379cb1
Source feed: FDA_Inspections

> FDA Inspection 1026856 for Renner & Co on September 28, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026856
- Company Name: Renner & Co
- Inspection Date: 2017-09-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1026856 - 2017-09-28](https://www.keypedia.com/records/fda_inspections/renner-co/026a45de-3879-4533-bc1f-2e76151dff29)
- [FDA Inspection 953257 - 2015-12-21](https://www.keypedia.com/records/fda_inspections/renner-co/20af4d62-3ba2-4a06-8c3b-3be5fdf93fd9)
- [FDA Inspection 953257 - 2015-12-21](https://www.keypedia.com/records/fda_inspections/renner-co/305a07ca-7b50-412e-8ecb-2e5842c64371)

Company: https://www.keypedia.com/companies/renner-co/67efdfd6-1e61-458d-83be-453276cd11a9

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