Englewood Lab Korea Co., Ltd. FDA Record

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

Englewood Lab Korea Co., Ltd. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Englewood Lab Korea Co., Ltd." is on file.

What these totals cover: FDA records filed under the name "Englewood Lab Korea Co., Ltd." and its spelling variant "Englewood Lab Korea Co".

Latest inspection
Oct 25, 2024 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Englewood Lab Korea Co., Ltd.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Englewood Lab Korea Co., Ltd.: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 0 inspections020232024: 1 inspections120242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202300000
202200000
202100000
202000000
201910000
201800000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

2 inspections from Jul 12, 2019 to Oct 25, 2024.

DateSiteProductClassificationFEI
Oct 25, 2024Namdong, Korea (The Republic Of)DrugsVoluntary Action Indicated (VAI)3013704938
Jul 12, 2019Namdong, Korea (The Republic Of)DrugsVoluntary Action Indicated (VAI)3013704938
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 3013704938Namdong, Korea (The Republic Of)2Oct 25, 2024

Englewood Lab Korea Co., Ltd. and the FDA: common questions

Has Englewood Lab Korea Co., Ltd. received an FDA warning letter?

No FDA warning letter addressed to the name "Englewood Lab Korea Co., Ltd." 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 Englewood Lab Korea Co., Ltd. received an FDA Form 483?

FDA has not published a Form 483 for "Englewood Lab Korea Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Englewood Lab Korea Co., Ltd.?

The most recent FDA inspection on file ended Oct 25, 2024 at Namdong, Korea (The Republic Of) and was classified VAI. FDA has 2 inspections of Englewood Lab Korea Co., Ltd. on file.

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