# Biofilm, Inc. – FDA Inspection, May 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/biofilm-inc/b382e90c-4223-48ee-99ae-2809175f0f40
Source feed: FDA_Inspections

> FDA inspection 1014535 of Biofilm, Inc., May 25, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014535
- Company Name: Biofilm, Inc.
- Inspection Date: 2017-05-25
- 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: 4

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## Related Officers

- [Theresa Kirkham](https://www.keypedia.com/people/theresa-kirkham/c7d8aad0-d162-4fac-a1ba-4649c36fd714)

Company: https://www.keypedia.com/companies/biofilm-inc/97b5de6b-0281-4eb7-afab-5a0f5dbde1f0

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