# Vineland Syrup Inc. – FDA Inspection, Nov 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/vineland-syrup-inc/8e2417d5-db7f-4758-8efb-9f14f2e6c358
Source feed: FDA_Inspections

> FDA inspection 1031950 of Vineland Syrup Inc., November 22, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031950
- Company Name: Vineland Syrup Inc.
- Inspection Date: 2017-11-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/brandon-l-mariner/c1ff0e66-552d-466a-9b49-a083d0211c94)
- [FDA Associated Person](https://www.keypedia.com/people/loretta-nemchik/37791f6d-862a-4863-9295-1cca43f9fe3a)

Company: https://www.keypedia.com/companies/vineland-syrup-inc/1763383b-d231-4929-b92b-5bf048103010

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7