# Perma Laboratories LLC – FDA Inspection, Jun 8, 2018

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

> FDA inspection 1055078 of Perma Laboratories LLC, June 08, 2018. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1055078
- Company Name: Perma Laboratories LLC
- Inspection Date: 2018-06-08
- 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: 10

## Related Documents

- [FDA Inspection 1329294 - 2026-08-04](https://www.keypedia.com/records/fda_inspections/perma-laboratories-llc/92a1b192-8a28-48d2-9f20-72e540961ee2)
- FDA Inspection 804595 - 2012-11-01
- [FDA Inspection 750306 - 2011-10-19](https://www.keypedia.com/records/fda_inspections/perma-laboratories-llc/62f6f868-b146-4235-82d9-d5c6bf90152d)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/benjamin-j-dastoli/688c2ad7-f7ac-47eb-8ca2-4efcd221f636)

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