North Hudson IVF Center For Fertility & Gynecology P.C. FDA Record

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

  • Latest inspection VAI · Jul 2, 2024
  • No warning letters matched by name
Inspections 7 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

North Hudson IVF Center For Fertility & Gynecology P.C. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "North Hudson IVF Center For Fertility & Gynecology P.C." is on file.

What these totals cover: FDA records filed under the name "North Hudson IVF Center For Fertility & Gynecology P.C." and its spelling variant "North Hudson Ivf Center For Fertility And Gynecology P.C".

Latest inspection
Jul 2, 2024 · VAI

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) clearances0Nov 15, 2026File dated Nov 9, 2026Current
Inspections7Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

North Hudson IVF Center For Fertility & Gynecology P.C.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

North Hudson IVF Center For Fertility & Gynecology P.C.: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202300000
202210000
202100000
202000000
201900000
201810000
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.

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Recent FDA inspections

7 inspections from Mar 31, 2009 to Jul 2, 2024.

DateSiteProductClassificationFEI
Jul 2, 2024Englewood Cliffs, NJBiologicsVoluntary Action Indicated (VAI)3003945116
Mar 3, 2022Englewood Cliffs, NJBiologicsNo Action Indicated (NAI)3003945116
Jun 11, 2018Englewood Cliffs, NJBiologicsNo Action Indicated (NAI)3003945116
Jul 18, 2016Englewood Cliffs, NJBiologicsNo Action Indicated (NAI)3003945116
Apr 3, 2014Englewood Cliffs, NJBiologicsVoluntary Action Indicated (VAI)3003945116
Oct 12, 2011Englewood Cliffs, NJBiologicsNo Action Indicated (NAI)3003945116
Mar 31, 2009Englewood Cliffs, NJBiologicsNo Action Indicated (NAI)3003945116
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 3003945116Englewood Cliffs, NJ7Jul 2, 2024

North Hudson IVF Center For Fertility & Gynecology P.C. and the FDA: common questions

Has North Hudson IVF Center For Fertility & Gynecology P.C. received an FDA warning letter?

No FDA warning letter addressed to the name "North Hudson IVF Center For Fertility & Gynecology P.C." 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 North Hudson IVF Center For Fertility & Gynecology P.C. received an FDA Form 483?

FDA has not published a Form 483 for "North Hudson IVF Center For Fertility & Gynecology P.C." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect North Hudson IVF Center For Fertility & Gynecology P.C.?

The most recent FDA inspection on file ended Jul 2, 2024 at Englewood Cliffs, NJ and was classified VAI. FDA has 7 inspections of North Hudson IVF Center For Fertility & Gynecology P.C. on file.

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