# FDA Inspection 893657 - Merz North America, Inc. - September 02, 2014

Source: https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/2433721f-b226-421b-b166-75b42d3a908e
Source feed: FDA_Inspections

> FDA Inspection 893657 for Merz North America, Inc. on September 02, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 893657
- Company Name: Merz North America, Inc.
- Inspection Date: 2014-09-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 893657 - 2014-09-02](https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/509083ac-d4b5-4268-8677-f16119303ff0)
- [FDA Inspection 834443 - 2013-04-19](https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/37db0a3f-65a7-470b-9730-c5b7c68f70b5)
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- [FDA Inspection 702452 - 2010-12-23](https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/2ea36a07-0581-4953-92c7-78ebc87f0f90)

Company: https://www.keypedia.com/companies/merz-north-america-inc/ee93b71a-c4d2-49d8-b449-c82b3df15397

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