# FDA Inspection 679136 - BUHLMANN Laboratories AG - August 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/buhlmann-laboratories-ag/b3a54204-5e17-41f1-90fc-4c88a86eb0ef
Source feed: FDA_Inspections

> FDA Inspection 679136 for BUHLMANN Laboratories AG on August 19, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 679136
- Company Name: BUHLMANN Laboratories AG
- Inspection Date: 2010-08-19
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 679136 - 2010-08-19](https://www.keypedia.com/records/fda_inspections/buhlmann-laboratories-ag/55e20150-6aa3-42df-bdd1-f9a028c20482)

Company: https://www.keypedia.com/companies/buhlmann-laboratories-ag/824ca9a6-83df-487d-9cb3-2842adcef213

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