# Merz North America, Inc. – FDA Inspection, Dec 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/2ea36a07-0581-4953-92c7-78ebc87f0f90
Source feed: FDA_Inspections

> FDA inspection 702452 of Merz North America, Inc., December 23, 2010. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 702452
- Company Name: Merz North America, Inc.
- Inspection Date: 2010-12-23
- 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: 7

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- [FDA Inspection 834443 - 2013-04-19](https://www.keypedia.com/records/fda_inspections/merz-north-america-inc/d5bca3e3-884d-4e8b-a09e-4a0b75c25fe5)
- FDA Inspection 715962 - 2011-04-08

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