# FDA Inspection 599121 - Merck KGaA - July 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/merck-kgaa/c5f114c3-c9d9-4b0e-85ca-a9c600a6078e
Source feed: FDA_Inspections

> FDA Inspection 599121 for Merck KGaA on July 02, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 599121
- Company Name: Merck KGaA
- Inspection Date: 2009-07-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/merck-kgaa/b5abb295-f221-4b66-9a49-d564f70c388b

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