# Renner & Co – FDA Inspection, Sep 28, 2017

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

> FDA inspection 1026856 of Renner & Co, September 28, 2017. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 8

## Related Documents

- [FDA Inspection 953257 - 2015-12-21](https://www.keypedia.com/records/fda_inspections/renner-co/305a07ca-7b50-412e-8ecb-2e5842c64371)

## Related Officers

- Issuing Officer

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