# DELBio, Inc. – FDA Inspection, Feb 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/delbio-inc/64ca16e4-e098-4373-9445-9d2eea803f44
Source feed: FDA_Inspections

> FDA inspection 1005973 of DELBio, Inc., February 16, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005973
- Company Name: DELBio, Inc.
- Inspection Date: 2017-02-16
- 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: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/thomas-a-peter/48a36892-cc03-42bb-8960-978d18f2147a)

Company: https://www.keypedia.com/companies/delbio-inc/88dd2edb-40cc-49ae-84cd-b90a62cce16a

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