FDA Inspection
Syntec Scientific CorporationSyntec Scientific Corporation – FDA Inspection, Jul 1, 2010
Record Details
This FDA Inspection record concerns Syntec Scientific Corporation, with an inspection on July 1, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 1, 2010
- Product Type
- Devices
View Company Profile
ID · f15156c1-0932-4d7b-a09d-3aa5c018a569
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 671677
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Syntec Scientific Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 26, 2026 | Not classified | Office of Inspections and Investigations | |
| May 5, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 13, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 18, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Syntec Scientific Corporation
- FDA Inspection 1315936 - 2026-03-26
- FDA Inspection 1207360 - 2023-05-05
- FDA Inspection 1081598 - 2018-12-13
- FDA Inspection 908743 - 2014-12-18
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