# FDA Inspection 658240 - Fiberoptic Components, LLC dba Innofiber - March 26, 2010

Source: https://www.keypedia.com/records/fda_inspections/fiberoptic-components-llc-dba-innofiber/b33db794-07c9-4ec1-9b77-0aca6a600088
Source feed: FDA_Inspections

> FDA Inspection 658240 for Fiberoptic Components, LLC dba Innofiber on March 26, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 658240
- Company Name: Fiberoptic Components, LLC dba Innofiber
- Inspection Date: 2010-03-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 612467 - 2009-09-16](https://www.keypedia.com/records/fda_inspections/fiberoptic-components-llc-dba-innofiber/8ea51633-ba5e-4e3e-b529-20d5819f8561)

Company: https://www.keypedia.com/companies/fiberoptic-components-llc-dba-innofiber/322e82f0-49a5-4c7a-b0fd-0848e9863ade

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