FDA Inspection
Perma Laboratories LLCPerma Laboratories LLC – FDA Inspection, Oct 19, 2011
Record Details
This FDA Inspection record concerns Perma Laboratories LLC, with an inspection on October 19, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Perma Laboratories LLC
- Inspection Date
- October 19, 2011
- Product Type
- Devices
View Company Profile
ID · 62f6f868-b146-4235-82d9-d5c6bf90152d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 750306
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.198(a)Complaints
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Perma Laboratories LLC
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 4, 2026 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 8, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 1, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Perma Laboratories LLC
- FDA Inspection 1329294 - 2026-08-04
- FDA Inspection 1055078 - 2018-06-08
- FDA Inspection 804595 - 2012-11-01
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.