# FDA Inspection 649401 - Hettich Instruments Lp - February 17, 2010

Source: https://www.keypedia.com/records/fda_inspections/hettich-instruments-lp/0f269372-44eb-45a8-8746-3f6ae93ea11c
Source feed: FDA_Inspections

> FDA Inspection 649401 for Hettich Instruments Lp on February 17, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 649401
- Company Name: Hettich Instruments Lp
- Inspection Date: 2010-02-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 649401 - 2010-02-17](https://www.keypedia.com/records/fda_inspections/hettich-instruments-lp/3c4d1f0d-53d9-44a7-ad21-6a1cde9ca9cc)

Company: https://www.keypedia.com/companies/hettich-instruments-lp/f2eed2e1-7d83-498e-9cdf-6be49d3f4f76

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