FDA Inspection
MECTA CorporationMECTA Corporation – FDA Inspection, Sep 1, 2009
Record Details
This FDA Inspection record concerns MECTA Corporation, with an inspection on September 1, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- MECTA Corporation
- Inspection Date
- September 1, 2009
- Product Type
- Devices
View Company Profile
ID · df28cd0c-b64a-4bad-a354-6acb6027601c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 604716
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
Full citation text and observation details available on the Dashboard.
Other FDA inspections of MECTA Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 30, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 15, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 2, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MECTA Corporation
- FDA Inspection 933861 - 2015-06-30
- FDA Inspection 822554 - 2013-03-15
- FDA Inspection 737273 - 2011-08-02
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