FDA Inspection
Vineland Syrup Inc.Vineland Syrup Inc. – FDA Inspection, Nov 22, 2017
Record Details
This FDA Inspection record concerns Vineland Syrup Inc., with an inspection on November 22, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 8e2417d5-db7f-4758-8efb-9f14f2e6c358
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1031950
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.25(b)Training records
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Vineland Syrup Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| March 4, 2024 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 8, 2020 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| January 26, 2018 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| February 10, 2015 | VAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| May 24, 2010 | VAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
Other documents for Vineland Syrup Inc.
- FDA Inspection 1231771 - 2024-03-04
- FDA Inspection 1131752 - 2020-09-08
- FDA Inspection 1052887 - 2018-01-26
- FDA Inspection 911661 - 2015-02-10
- FDA Inspection 661956 - 2010-05-24
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