GE Inspection Technologies, LP
GE Inspection Technologies, LP has 6 FDA enforcement events on this register (7 product records) between 2014 and 2017: 6 device; the busiest year was 2014 with 2.
0% of its events are Class I; the most common class is Class II (6). 0 events are listed as ongoing; the recalling firm's address is in PA.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 28 Jun 2017 | GE Inspection Technologies Blade|line Industrial Cabinet X-ray system | Device | Class II | 1 | Terminated |
| 2 Mar 2016 | GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis. | Device | Class II | 1 | Terminated |
| 16 Dec 2015 | GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control. | Device | Class II | 1 | Terminated |
| 13 Jan 2015 | GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system | Device | Class II | 2 | Terminated |
| 10 Nov 2014 | GE Optional Laser Centering Device X-ray generator. | Device | Class II | 1 | Terminated |
| 10 Nov 2014 | GE Cabinet X-ray systems | Device | Class II | 1 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has GE Inspection Technologies, LP had?
6 enforcement events (7 product records) on this register, 2014–2017: 6 device.
Are any GE Inspection Technologies, LP recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are GE Inspection Technologies, LP recalls?
6 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.