# FDA Inspection 953257 - Renner & Co - December 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/renner-co/20af4d62-3ba2-4a06-8c3b-3be5fdf93fd9
Source feed: FDA_Inspections

> FDA Inspection 953257 for Renner & Co on December 21, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953257
- Company Name: Renner & Co
- Inspection Date: 2015-12-21
- Classification: Official Action Indicated (OAI)
- 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/renner-co/67efdfd6-1e61-458d-83be-453276cd11a9

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