# FDA Inspection 1039330 - Sun Capsule Corporation - February 01, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/sun-capsule-corporation/282693ef-2e62-4c37-884f-240623ddac89
Source feed: FDA_Inspections

> FDA Inspection 1039330 for Sun Capsule Corporation on February 01, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1039330
- Company Name: Sun Capsule Corporation
- Inspection Date: 2018-02-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1039330 - 2018-02-01](https://www.globalkeysolutions.net/records/fda_inspections/sun-capsule-corporation/32eb877e-730e-456b-812a-3b182f91fcc3)
- [FDA Inspection 1039330 - 2018-02-01](https://www.globalkeysolutions.net/records/fda_inspections/sun-capsule-corporation/c9ff4e7a-86ef-4564-92fb-a9c8a8870113)

Company: https://www.globalkeysolutions.net/companies/sun-capsule-corporation/0c9f50ab-6023-4976-a04f-0363bc6e5cf3

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