# FDA Inspection 1036261 - Microtek Dominicana, S.A. - August 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/microtek-dominicana-sa/d386a07a-f0ad-4155-ab0c-4c3bc029256b
Source feed: FDA_Inspections

> FDA Inspection 1036261 for Microtek Dominicana, S.A. on August 16, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1036261
- Company Name: Microtek Dominicana, S.A.
- Inspection Date: 2017-08-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 569111 - 2009-01-29](https://www.keypedia.com/records/fda_inspections/microtek-dominicana-sa/9d290214-f85d-4dce-bd97-59180b697738)

Company: https://www.keypedia.com/companies/microtek-dominicana-sa/5bd0f123-028e-4562-b578-2ba0c8d099c6

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