FDA Inspection
Molded Products IncMolded Products Inc – FDA Inspection, Feb 14, 2013
Record Details
This FDA Inspection record concerns Molded Products Inc, with an inspection on February 14, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Molded Products Inc
- Inspection Date
- February 14, 2013
- Product Type
- Devices
View Company Profile
ID · 3a5dc571-139a-4dbc-ba92-0522d72a077a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 818491
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 806.10(a)(2)Report of violation of the Act (see 803.52(e)(9))
- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Molded Products Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 7, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 11, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 10, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 26, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Molded Products Inc
- FDA Inspection 1182078 - 2022-10-07
- FDA Inspection 1050201 - 2018-04-11
- FDA Inspection 1005518 - 2017-03-10
- FDA Inspection 579746 - 2009-03-26
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