# Perma Pure LLC – FDA Inspection, Aug 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/perma-pure-llc/de0be5b0-626d-43ff-b9a6-f39ad8f8b1e4
Source feed: FDA_Inspections

> FDA inspection 675749 of Perma Pure LLC, August 23, 2010. Classification: Official Action Indicated (OAI). 12 citations under 21 CFR parts 803 and 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675749
- Company Name: Perma Pure LLC
- Inspection Date: 2010-08-23
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

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Company: https://www.keypedia.com/companies/perma-pure-llc/73139477-c364-4c3c-a881-0f88d8a57088

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