# FDA Inspection 828392 - Merz North America, Inc. - April 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/eaa1092f-af84-4f47-8553-49cc3624dc75
Source feed: FDA_Inspections

> FDA Inspection 828392 for Merz North America, Inc. on April 19, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 828392
- Company Name: Merz North America, Inc.
- Inspection Date: 2013-04-19
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1226927 - 2024-01-03](https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/fa90c204-a476-48c0-8260-4b87a4f1b8c4)

Company: https://www.keypedia.com/companies/merz-north-america-inc/e183daff-93f0-4f77-a3e2-f7a8d9e50d1f

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