# Capsule Tech, Inc – FDA Inspection, Jun 16, 2011

Source: https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/5a043e14-22c2-4eb3-a95a-0462f459ca2a
Source feed: FDA_Inspections

> FDA inspection 730415 of Capsule Tech, Inc, June 16, 2011. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 730415
- Company Name: Capsule Tech, Inc
- Inspection Date: 2011-06-16
- 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: 2

## Related Documents

- [FDA Inspection 1109050 - 2018-10-26](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/6984b3b1-0bb0-4a23-9870-fd78552d1476)
- [FDA Inspection 989624 - 2016-10-20](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/d86ae548-314a-484e-905b-fca95c75ceec)
- [FDA Inspection 989623 - 2016-10-20](https://www.keypedia.com/records/fda_inspections/capsule-tech-inc/bce03faf-f2b6-47d4-9eea-26f404dbbfe4)
- FDA Inspection 866410 - 2014-02-18

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