Home / Facilities / 3027608029

Lindsey Roeker, M.D. — FDA Facility Profile

FEI 3027608029

Lindsey Roeker, M.D. is an FDA-inspected facility (FEI 3027608029) located in New York, NY, US. RegDataLab tracks 1 FDA inspection at this facility.

Reviewing Lindsey Roeker, M.D. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Lindsey Roeker, M.D. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Latest inspection
Sep 12, 2023: No Action Indicated (NAI)
Inspections on record
1 (1 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Sep 12, 2023No Action Indicated (NAI)No citations listed

Facility details

Company
Lindsey Roeker, M.D.
Location
New York, NY (US)
Source
inspections

FDA data resources

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