# FDA Inspection 803122 - Biomatlante - September 13, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/biomatlante/fb949d68-0535-4b87-b286-e1bf68079f1a/
Source feed: FDA_Inspections

> FDA Inspection 803122 for Biomatlante on September 13, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803122
- Company Name: Biomatlante
- Inspection Date: 2012-09-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/biomatlante/994744bd-efae-4c15-be8c-e6ca7c4893bd

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