# FDA Inspection 1239187 - Fiberoptic Technology, Inc. - May 03, 2024

Source: https://www.keypedia.com/records/fda_inspections/fiberoptic-technology-inc/4cf0460c-2bd5-4552-9b23-7fd9b0162aac
Source feed: FDA_Inspections

> FDA Inspection 1239187 for Fiberoptic Technology, Inc. on May 03, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1239187
- Company Name: Fiberoptic Technology, Inc.
- Inspection Date: 2024-05-03
- 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 1239187 - 2024-05-03](https://www.keypedia.com/records/fda_inspections/fiberoptic-technology-inc/51639fdd-5a72-476a-8c61-70e1c42d9b89)
- [FDA Inspection 1013064 - 2017-04-28](https://www.keypedia.com/records/fda_inspections/fiberoptic-technology-inc/16a9f492-fd51-41f0-a255-d368139559e0)

Company: https://www.keypedia.com/companies/fiberoptic-technology-inc/d46055ba-944e-4dd3-aa9e-69c69ad0ef3a

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