# FDA Inspection 805507 - Metoxit AG - September 12, 2012

Source: https://www.keypedia.com/records/fda_inspections/metoxit-ag/c15cb74e-340c-40c4-8d71-4dbe6be6c102
Source feed: FDA_Inspections

> FDA Inspection 805507 for Metoxit AG on September 12, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805507
- Company Name: Metoxit AG
- Inspection Date: 2012-09-12
- 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/metoxit-ag/121e038d-b973-428e-bde8-f17024d927dd

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