# Boss Instruments, Ltd. – FDA Inspection, Jun 28, 2018

Source: https://www.keypedia.com/records/fda_inspections/boss-instruments-ltd/8d1a192d-2636-41f1-9c6e-ca6d7394a94f
Source feed: FDA_Inspections

> FDA inspection 1057387 of Boss Instruments, Ltd., June 28, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057387
- Company Name: Boss Instruments, Ltd.
- Inspection Date: 2018-06-28
- 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: 3

## Related Documents

- FDA Inspection 730785 - 2011-06-21

## Related Officers

- [Tiki Dixon](https://www.keypedia.com/people/tiki-dixon/b3160a2c-ef16-4fa2-b9b9-4c3a0ed17c5b)

Company: https://www.keypedia.com/companies/boss-instruments-ltd/eea4a75b-0ac4-4e43-828d-88f0f976934d

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