# Fiberoptic Technology, Inc. – FDA Inspection, Apr 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/fiberoptic-technology-inc/16a9f492-fd51-41f0-a255-d368139559e0
Source feed: FDA_Inspections

> FDA inspection 1013064 of Fiberoptic Technology, Inc., April 28, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013064
- Company Name: Fiberoptic Technology, Inc.
- Inspection Date: 2017-04-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1327746 - 2026-07-24](https://www.keypedia.com/records/fda_inspections/fiberoptic-technology-inc/b23ccf9d-96f3-4a32-85e0-7e213e5b5998)
- [FDA Inspection 1239187 - 2024-05-03](https://www.keypedia.com/records/fda_inspections/fiberoptic-technology-inc/51639fdd-5a72-476a-8c61-70e1c42d9b89)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/eric-c-schmitt/f2716c8c-f06e-4519-a1e7-63a3ef6e07fb)

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