FDA Inspection
E. Benson Hood Laboratories, Inc.E. Benson Hood Laboratories, Inc. – FDA Inspection, Feb 20, 2024
Record Details
This FDA Inspection record concerns E. Benson Hood Laboratories, Inc., with an inspection on February 20, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 9f9d8ce1-230c-4b2a-904e-2a58bba3e334
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1230777
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.80(e)Documentation
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of E. Benson Hood Laboratories, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 31, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 21, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 31, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for E. Benson Hood Laboratories, Inc.
- FDA Inspection 1041755 - 2018-01-31
- FDA Inspection 809401 - 2012-12-21
- FDA Inspection 604392 - 2009-08-31
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