FDA Inspection
Action Products IncorporatedAction Products Incorporated – FDA Inspection, Sep 19, 2014
Record Details
This FDA Inspection record concerns Action Products Incorporated, with an inspection on September 19, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Action Products Incorporated
- Inspection Date
- September 19, 2014
- Product Type
- Devices
View Company Profile
ID · 9aeeffff-072a-41c7-aa14-f519aa269df6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 896217
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.22Quality Audit/Reaudit - conducted
- 21 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
- 21 CFR 803.17(a)(2)Lack of System for Determining MDR Events
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Action Products Incorporated
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 11, 2025 | Not classified | Baltimore District Office | |
| December 7, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 9, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Action Products Incorporated
- FDA Inspection 1272601 - 2025-06-11
- FDA Inspection 1034224 - 2017-12-07
- FDA Inspection 740562 - 2011-08-09
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.