FDA Inspection
Plasti Products IncPlasti Products Inc – FDA Inspection, Dec 9, 2016
Record Details
This FDA Inspection record concerns Plasti Products Inc, with an inspection on December 9, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- People
- Eric C. Fox (Investigator)
- Mary K. Concannon (Issuing Officer)
View Company Profile
ID · e3c0fae2-9384-47ee-a77c-4b35c9255d89
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1018322
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Plasti Products Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 25, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 30, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 28, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 17, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Plasti Products Inc
- FDA Inspection 1207693 - 2023-05-25
- FDA Inspection 815974 - 2013-01-30
- FDA Inspection 816224 - 2013-01-28
- FDA Inspection 706915 - 2010-12-17
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.