FDA Inspection
Bonasse Enterprises Co., Ltd.Bonasse Enterprises Co., Ltd. – FDA Inspection, Feb 11, 2015
Record Details
This FDA Inspection record concerns Bonasse Enterprises Co., Ltd., with an inspection on February 11, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 11, 2015
- Product Type
- Devices
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ID · d49f9a6d-b485-4788-b7c6-3624dc165876
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 915772
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.40Procedures not adequately established or maintained
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Other FDA inspections of Bonasse Enterprises Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 13, 2025 | Not classified | Office of Inspections and Investigations | |
| August 20, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bonasse Enterprises Co., Ltd.
- FDA Inspection 1264293 - 2025-02-13
- FDA Inspection 683833 - 2010-08-20
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