# FDA Inspection 989624 - Capsule Tech, Inc - October 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/658d2ac3-76f0-4c01-9eb3-fe6e50a088ee
Source feed: FDA_Inspections

> FDA Inspection 989624 for Capsule Tech, Inc on October 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989624
- Company Name: Capsule Tech, Inc
- Inspection Date: 2016-10-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 989623 - 2016-10-20](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/bce03faf-f2b6-47d4-9eea-26f404dbbfe4)
- [FDA Inspection 989623 - 2016-10-20](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/50b84edf-0846-41b3-8694-9927be9c0a37)
- [FDA Inspection 989624 - 2016-10-20](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/d86ae548-314a-484e-905b-fca95c75ceec)
- [FDA Inspection 866410 - 2014-02-18](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/d5876032-56f2-463a-9081-fa19745b3338)
- [FDA Inspection 866410 - 2014-02-18](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/0f58a7ba-fdf3-4e51-9026-e7b1c9afb37e)

Company: https://www.keypedia.com/companies/capsule-tech-inc/96a55558-2d91-449b-839d-d193506f4eac

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