Transverse Industries Co. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • Latest inspection NAI · Apr 8, 2009
  • No warning letters matched by name
Inspections 1 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 1 Latest Oct 10, 2007

Transverse Industries Co. has 0 FDA recalls, 1 inspection, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Transverse Industries Co." is on file.

What these totals cover: FDA records filed under the name "Transverse Industries Co." and its spelling variants "Transverse Industries", "Transverse Industries Co".

Latest inspection
Apr 8, 2009 · NAI
Latest 510(k)
Oct 10, 2007

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances1Nov 15, 2026File dated Nov 9, 2026Current
Inspections1Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

1 inspection on Apr 8, 2009.

DateSiteProductClassificationFEI
Apr 8, 2009New Taipei City, TaiwanDevicesNo Action Indicated (NAI)1000284205
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1000284205New Taipei City, Taiwan1Apr 8, 2009

Recent 510(k) clearances

1 510(k) clearance on Oct 10, 2007.

K-NumberDeviceDate
K070870SKIN CARE LIGHTOct 10, 2007

Transverse Industries Co. and the FDA: common questions

Has Transverse Industries Co. received an FDA warning letter?

No FDA warning letter addressed to the name "Transverse Industries Co." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Transverse Industries Co. received an FDA Form 483?

FDA has not published a Form 483 for "Transverse Industries Co." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Transverse Industries Co.?

The most recent FDA inspection on file ended Apr 8, 2009 at New Taipei City, Taiwan and was classified NAI. FDA has 1 inspection of Transverse Industries Co. on file.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.