FDA Inspection
Linemaster Switch CorporationLinemaster Switch Corporation – FDA Inspection, Jan 12, 2012
Record Details
This FDA Inspection record concerns Linemaster Switch Corporation, with an inspection on January 12, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 12, 2012
- Product Type
- Devices
View Company Profile
ID · 80737440-13df-402e-9ad1-69c6c6b5483a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 768698
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.40(a)Not approved or obsolete document retrieval
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.50(a)(1)Documented evaluation
- 21 CFR 820.30(g)Design validation - documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Linemaster Switch Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 6, 2026 | OAI | New England District Office | Compliance: Devices |
| February 15, 2023 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 12, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 1, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Linemaster Switch Corporation
- FDA Inspection 1306502 - 2026-03-06
- FDA Inspection 1199731 - 2023-02-15
- FDA Inspection 1051163 - 2018-04-12
- FDA Inspection 899750 - 2014-10-01
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.