FDA Inspection
Molded Products IncMolded Products Inc – FDA Inspection, Mar 26, 2009
Record Details
This FDA Inspection record concerns Molded Products Inc, with an inspection on March 26, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Molded Products Inc
- Inspection Date
- March 26, 2009
- Product Type
- Devices
View Company Profile
ID · cdd7a3f1-06fb-455e-bf27-d02e07eaf401
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 579746
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
6- 21 CFR 820.80(e)Documentation
- 21 CFR 820.80(c)Lack of or inadequate In-process acceptance procedures
- 21 CFR 820.72(a)Equipment suitability & capability
- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.70(a)Process control procedures
- 21 CFR 820.90(b)(1)Documentation of disposition, justification, signature
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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 |
| February 14, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: 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 818491 - 2013-02-14
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