FDA Inspection
Vectec S.A.Vectec S.A. – FDA Inspection, Jul 19, 2013
Record Details
This FDA Inspection record concerns Vectec S.A., with an inspection on July 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Vectec S.A.
- Inspection Date
- July 19, 2013
- Product Type
- Devices
View Company Profile
ID · 8979135c-900f-42ec-869e-f26ca27633c4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 842115
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(a)General
- 21 CFR 820.30(a)Design control - no procedures
- 21 CFR 820.90(a)Nonconforming product control
- 21 CFR 820.100(a)Lack of or inadequate procedures
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