# Acro Biotech Inc. – FDA Inspection, May 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/acro-biotech-inc/cff77bf3-b41f-45a9-9283-85a0a321bc8f
Source feed: FDA_Inspections

> FDA inspection 1050458 of Acro Biotech Inc., May 01, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050458
- Company Name: Acro Biotech Inc.
- Inspection Date: 2018-05-01
- 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 Documents

- FDA Inspection 850016 - 2013-09-03

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sonya-l-karsik/c24603b9-5ca0-46f5-861a-b367155b0def)

Company: https://www.keypedia.com/companies/acro-biotech-inc/2591a2ab-9c6e-49ca-8e26-ee9988a22eb5

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