# FDA Inspection 1210591 - Whele LLC DBA Perch - July 18, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/whele-llc-dba-perch/4800669e-465f-4e18-bac3-6b1bd8d85bc0
Source feed: FDA_Inspections

> FDA Inspection 1210591 for Whele LLC DBA Perch on July 18, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210591
- Company Name: Whele LLC DBA Perch
- Inspection Date: 2023-07-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1210591 - 2023-07-18](https://www.globalkeysolutions.net/records/fda_inspections/whele-llc-dba-perch/6844afd8-cd8a-4c1b-ac9e-8de8b47a8953)
- [FDA Inspection 1171317 - 2022-06-06](https://www.globalkeysolutions.net/records/fda_inspections/whele-llc-dba-perch/a9ca8d15-e045-4799-a60e-045b4616d338)
- [FDA Inspection 1171317 - 2022-06-06](https://www.globalkeysolutions.net/records/fda_inspections/whele-llc-dba-perch/c0acfff3-5433-419f-b07a-f2e547e6f616)

Company: https://www.globalkeysolutions.net/companies/whele-llc-dba-perch/114a5f37-7375-4993-a6e2-7d5fb921e537

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