# Plasti Products Inc – FDA Inspection, Dec 9, 2016

Source: https://www.keypedia.com/records/fda_inspections/plasti-products-inc/e3c0fae2-9384-47ee-a77c-4b35c9255d89
Source feed: FDA_Inspections

> FDA inspection 1018322 of Plasti Products Inc, December 09, 2016. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018322
- Company Name: Plasti Products Inc
- Inspection Date: 2016-12-09
- 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: 0

## Related Documents

- FDA Inspection 1207693 - 2023-05-25
- [FDA Inspection 815974 - 2013-01-30](https://www.keypedia.com/records/fda_inspections/plasti-products-inc/8e955970-6cdd-4288-8c85-855f943e0992)
- FDA Inspection 816224 - 2013-01-28
- FDA Inspection 706915 - 2010-12-17

## Related Officers

- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)
- Issuing Officer

Company: https://www.keypedia.com/companies/plasti-products-inc/65a72052-1d9e-4cc6-8dff-fd28a31d137e

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