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FDA Inspection
•Biofilm, Inc.•June 15, 2023

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

Record Details

This FDA Inspection record concerns Biofilm, Inc., with an inspection on June 15, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Biofilm, Inc.
Inspection Date
June 15, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Sarah A. Hassas (Company Rep)
View Company Profile

ID · db6cfc91-a81d-4bdb-82c6-2cbe98a4a653

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1210051
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Biofilm, Inc.

4
DateClassificationOfficeProject area
May 19, 2026Not classifiedLos Angeles District OfficePostmarket Assurance: Devices
May 25, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
September 14, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
June 1, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Biofilm, Inc.
  • FDA Inspection 1318370 - 2026-05-19
  • FDA Inspection 1014535 - 2017-05-25
  • FDA Inspection 745757 - 2011-09-14
  • FDA Inspection 727215 - 2011-06-01

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