# Biofilm, Inc. – FDA Inspection, Jun 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/biofilm-inc/db6cfc91-a81d-4bdb-82c6-2cbe98a4a653
Source feed: FDA_Inspections

> FDA inspection 1210051 of Biofilm, Inc., June 15, 2023. Classification: No Action Indicated (NAI). Form 483 issued. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1210051
- Company Name: Biofilm, Inc.
- Inspection Date: 2023-06-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1318370 - 2026-05-19](https://www.keypedia.com/records/fda_inspections/biofilm-inc/4b8eacdc-2767-4794-ab2c-e5c4a9d32ec7)
- [FDA Inspection 1014535 - 2017-05-25](https://www.keypedia.com/records/fda_inspections/biofilm-inc/b382e90c-4223-48ee-99ae-2809175f0f40)
- FDA Inspection 745757 - 2011-09-14
- [FDA Inspection 727215 - 2011-06-01](https://www.keypedia.com/records/fda_inspections/biofilm-inc/47e1d78b-771b-4a1e-95d6-52d26aced4b8)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

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