# Fresenius Kabi Warrendale – FDA Inspection, Sep 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/fresenius-kabi-warrendale/b981ba4b-be16-4378-b1bc-1af55ea724f7
Source feed: FDA_Inspections

> FDA inspection 1030393 of Fresenius Kabi Warrendale, September 14, 2017. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030393
- Company Name: Fresenius Kabi Warrendale
- Inspection Date: 2017-09-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1237140 - 2024-04-16
- [FDA Inspection 924837 - 2015-05-05](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-warrendale/950181f1-d337-4887-adf6-f8dbdf334748)
- FDA Inspection 812876 - 2012-12-20
- FDA Inspection 735611 - 2011-05-27
- FDA Inspection 541136 - 2008-10-07

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/katelyn-a-staub-zamperini/bb7f95a4-53c1-473c-856e-517312bdba30)

Company: https://www.keypedia.com/companies/fresenius-kabi-warrendale/b2524c54-2bb4-4977-9ea7-d82266551b76

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