FDA Inspection
Molded Products IncMolded Products Inc – FDA Inspection, Mar 10, 2017
Record Details
This FDA Inspection record concerns Molded Products Inc, with an inspection on March 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 87afd57f-2abd-47d4-84bf-ccbe77bb90a7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1005518
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 806.10(a)(2)Report of violation of the Act (see 803.52(e)(9))
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 |
| February 14, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: 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 818491 - 2013-02-14
- FDA Inspection 579746 - 2009-03-26
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