# FDA Inspection 900143 - Erbe USA Inc - October 14, 2014

Source: https://www.keypedia.com/records/fda_inspections/erbe-usa-inc/71c5282d-fafe-4a9b-a406-0c948231e33e
Source feed: FDA_Inspections

> FDA Inspection 900143 for Erbe USA Inc on October 14, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900143
- Company Name: Erbe USA Inc
- Inspection Date: 2014-10-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/erbe-usa-inc/3ee94bb4-09e0-4480-87e1-9a8b8b3279b2

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