FDA Inspection
Temec Instruments B.V.Temec Instruments B.V. – FDA Inspection, Nov 24, 2011
Record Details
This FDA Inspection record concerns Temec Instruments B.V., with an inspection on November 24, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Temec Instruments B.V.
- Inspection Date
- November 24, 2011
- Product Type
- Devices
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ID · 57e3758d-a2b7-4e19-80b3-5818118f2bfb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 755350
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.30(g)Design validation - user needs and intended uses
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