# FDA Inspection 1022007 - Higi SH LLC - August 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/higi-sh-llc/5d776d24-942c-4e69-b16c-f7808786ea2a
Source feed: FDA_Inspections

> FDA Inspection 1022007 for Higi SH LLC on August 17, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022007
- Company Name: Higi SH LLC
- Inspection Date: 2017-08-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1022007 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/higi-sh-llc/2dbf67b3-e9e0-4b9e-86ea-f57991c33393)
- [FDA Inspection 847992 - 2013-09-04](https://www.keypedia.com/records/fda_inspections/higi-sh-llc/77b05a5a-daab-4bb5-8f39-03cd56dee48c)

Company: https://www.keypedia.com/companies/higi-sh-llc/586484ec-098d-4343-86d4-bcc797b4dc2a

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