# Renner & Co – FDA Inspection, Dec 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/renner-co/305a07ca-7b50-412e-8ecb-2e5842c64371
Source feed: FDA_Inspections

> FDA inspection 953257 of Renner & Co, December 21, 2015. Classification: Official Action Indicated (OAI). 7 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 953257
- Company Name: Renner & Co
- Inspection Date: 2015-12-21
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 1026856 - 2017-09-28](https://www.keypedia.com/records/fda_inspections/renner-co/e0a7c4cf-b7ab-4997-b28c-66cb58379cb1)

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