FDA Inspection
IDS Co., LTDIDS Co., LTD – FDA Inspection, Nov 8, 2019
Record Details
This FDA Inspection record concerns IDS Co., LTD, with an inspection on November 8, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- IDS Co., LTD
- Inspection Date
- November 8, 2019
- Product Type
- Devices
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ID · ce7635ed-6e4b-47a6-9d0e-d3b8ffbd796a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1109767
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of IDS Co., LTD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 6, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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