# FDA Inspection 888754 - Ulrich Gmbh & Co. KG - July 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/ulrich-gmbh-co-kg/61d62b4e-baee-4fb0-911d-f423c68bf2c2
Source feed: FDA_Inspections

> FDA inspection 888754 of Ulrich Gmbh & Co. KG, July 10, 2014. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 888754
- Company Name: Ulrich Gmbh & Co. KG
- Inspection Date: 2014-07-10
- 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 833997 - 2013-05-03](https://www.keypedia.com/records/fda_inspections/ulrich-gmbh-co-kg/a18175aa-f158-4050-8099-b79c37f8c475)
- FDA Inspection 667946 - 2010-06-10

Company: https://www.keypedia.com/companies/ulrich-gmbh-co-kg/01d10e71-d15b-45b0-a8ac-422de139ffe0

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