# FDA Inspection 631160 - Stihler Electronic Gmbh - November 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/stihler-electronic-gmbh/8f19ec8c-34c1-458a-b1b0-228d9a5e3e7e
Source feed: FDA_Inspections

> FDA Inspection 631160 for Stihler Electronic Gmbh on November 09, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 631160
- Company Name: Stihler Electronic Gmbh
- Inspection Date: 2009-11-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 902860 - 2014-10-27](https://www.keypedia.com/records/fda_inspections/stihler-electronic-gmbh/ee65a017-f7f8-4a2c-ba40-3fecaa0c686a)
- [FDA Inspection 631160 - 2009-11-09](https://www.keypedia.com/records/fda_inspections/stihler-electronic-gmbh/88a3bec2-daf4-4069-942a-2420b723fd43)

Company: https://www.keypedia.com/companies/stihler-electronic-gmbh/3cb2d870-bc16-4a08-b78d-5d78b2951d71

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