FDA Inspection
Biofilm, Inc.Biofilm, Inc. – FDA Inspection, May 19, 2026
Record Details
This FDA Inspection record concerns Biofilm, Inc., with an inspection on May 19, 2026, issued by the Los Angeles District Office, covering medical devices & rad health.
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ID · 4b8eacdc-2767-4794-ab2c-e5c4a9d32ec7
Inspection Facts
- Inspection number
- 1318370
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Biofilm, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 25, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 14, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 1, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Biofilm, Inc.
- FDA Inspection 1210051 - 2023-06-15
- FDA Inspection 1014535 - 2017-05-25
- FDA Inspection 745757 - 2011-09-14
- FDA Inspection 727215 - 2011-06-01
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