# MECTA Corporation – FDA Inspection, Sep 1, 2009

Source: https://www.keypedia.com/records/fda_inspections/mecta-corporation/df28cd0c-b64a-4bad-a354-6acb6027601c
Source feed: FDA_Inspections

> FDA inspection 604716 of MECTA Corporation, September 01, 2009. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 604716
- Company Name: MECTA Corporation
- Inspection Date: 2009-09-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 933861 - 2015-06-30
- [FDA Inspection 822554 - 2013-03-15](https://www.keypedia.com/records/fda_inspections/mecta-corporation/8f1afd6e-1745-4afd-8bef-38ebcd7fd582)
- FDA Inspection 737273 - 2011-08-02

Company: https://www.keypedia.com/companies/mecta-corporation/58c14e8a-cc3c-4103-9b53-8bc6dea3cae5

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7