# Tedec-Meiji Farma, S.A. – FDA Inspection, Dec 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/tedec-meiji-farma-sa/08ab45d9-75fe-4b73-ad86-87d50403df04
Source feed: FDA_Inspections

> FDA inspection 996370 of Tedec-Meiji Farma, S.A., December 15, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 996370
- Company Name: Tedec-Meiji Farma, S.A.
- Inspection Date: 2016-12-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 908026 - 2014-12-12
- [FDA Inspection 809541 - 2012-11-22](https://www.keypedia.com/records/fda_inspections/tedec-meiji-farma-sa/e73b1703-ce33-4d0d-a4e4-78e8bcd6aa71)
- [FDA Inspection 741672 - 2011-07-22](https://www.keypedia.com/records/fda_inspections/tedec-meiji-farma-sa/5cdcd4fb-2023-4ad1-bfd8-1e2bdeafa34a)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/tedec-meiji-farma-sa/8cd12cc2-f101-46d8-b715-8ff0b37fb759

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