# Ulrich Medical USA Inc – FDA Inspection, Jan 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/ulrich-medical-usa-inc/506e9012-ad0d-40aa-b2e1-c41e14e12f75
Source feed: FDA_Inspections

> FDA inspection 998483 of Ulrich Medical USA Inc, January 12, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998483
- Company Name: Ulrich Medical USA Inc
- Inspection Date: 2017-01-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1264134 - 2025-03-17](https://www.keypedia.com/records/fda_inspections/ulrich-medical-usa-inc/8e89dab0-1844-4b19-af64-f8e746c22239)
- [FDA Inspection 1083130 - 2019-03-06](https://www.keypedia.com/records/fda_inspections/ulrich-medical-usa-inc/ac9284c3-4c12-499b-b124-b11b23b461eb)
- FDA Inspection 649521 - 2010-02-25

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)
- [Company Rep](https://www.keypedia.com/people/karen-m-montgomery/ee91b1bb-8d51-4fdc-bee5-949441136e59)

Company: https://www.keypedia.com/companies/ulrich-medical-usa-inc/218cceea-167a-4243-9eae-433d78dae9ab

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