# CEA Global Dominicana d.b.a. Nissha Medical Technologies, San Pedro de Macoris, Dominican Republic (the) – FDA Inspections

Source: https://www.keypedia.com/companies/cea-global-dominicana-dba-nissha-medical-technologies/6d45cf1e-2a91-44fb-a304-ae575e0e4ed0

> Inspection records and compliance data for CEA Global Dominicana d.b.a. Nissha Medical Technologies in San Pedro de Macoris. 3 FDA inspections on record, last inspected February 07, 2019.

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## Details

- Name: CEA Global Dominicana d.b.a. Nissha Medical Technologies
- FEI Number: 3006891611
- Address Line 1: Zona Franca Industrial
- City: San Pedro de Macoris
- Country Name: Dominican Republic (the)
- Address: Zona Franca Industrial, San Pedro de Macoris, Dominican Republic (the)
- Country: Dominican Republic (the)

## Related Documents

- [FDA Inspection 1083033 - CEA Global Dominicana d.b.a. Nissha Medical Technologies - 2019-02-07](https://www.keypedia.com/records/fda_inspections/cea-global-dominicana-dba-nissha-medical-technologies/d9b946df-ee3d-4e0f-a41f-1f5928950720) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2019
- [FDA Inspection 969808 - CEA Global Dominicana d.b.a. Nissha Medical Technologies - 2016-04-14](https://www.keypedia.com/records/fda_inspections/cea-global-dominicana-dba-nissha-medical-technologies/f79c5416-cc26-43ae-96ce-57bf3ebd1a72) — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2016
- FDA Inspection 969808 - CEA Global Dominicana d.b.a. Nissha Medical Technologies - 2016-04-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 14, 2016
- [FDA Inspection 770919 - CEA Global Dominicana d.b.a. Nissha Medical Technologies - 2012-02-02](https://www.keypedia.com/records/fda_inspections/cea-global-dominicana-dba-nissha-medical-technologies/9695d381-192f-496a-bc85-108887b61805) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2012
- FDA Inspection 770919 - CEA Global Dominicana d.b.a. Nissha Medical Technologies - 2012-02-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2012

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