# FDA Inspection 1055078 - Perma Laboratories LLC - June 08, 2018

Source: https://www.keypedia.com/records/fda_inspections/perma-laboratories-llc/2abcb6a6-f214-4ca4-99f5-1a6c8d936f7f
Source feed: FDA_Inspections

> FDA Inspection 1055078 for Perma Laboratories LLC on June 08, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055078
- Company Name: Perma Laboratories LLC
- Inspection Date: 2018-06-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1055078 - 2018-06-08](https://www.keypedia.com/records/fda_inspections/perma-laboratories-llc/029755f9-89f9-4111-81d1-6ef197b19936)
- [FDA Inspection 804595 - 2012-11-01](https://www.keypedia.com/records/fda_inspections/perma-laboratories-llc/6009290e-8b57-432f-9347-079425e8f6ab)
- [FDA Inspection 750306 - 2011-10-19](https://www.keypedia.com/records/fda_inspections/perma-laboratories-llc/62f6f868-b146-4235-82d9-d5c6bf90152d)

Company: https://www.keypedia.com/companies/perma-laboratories-llc/20bbf9c2-3934-4b05-9991-c249ca905afa

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