Home / Facilities / 3033274216

RETMAP, INC. — FDA Facility Profile

FEI 3033274216

RETMAP, INC. is an FDA-registered facility (FEI 3033274216) located in Chicago, IL, US. RegDataLab tracks 1 FDA inspection at this facility.

Reviewing RETMAP, INC. 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 RETMAP, INC. 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
Oct 30, 2025: Voluntary Action Indicated (VAI)
Inspections on record
1 (1 VAI)
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
Oct 30, 2025Voluntary Action Indicated (VAI)Acceptable supplier records, inadequate records (21 CFR 820.50(a)(3))
Lack of or inadequate procedures (21 CFR 820.100(a))
Equipment control activity documentation (21 CFR 820.72(a))
Nonconforming product, Lack of or inadequate procedures (21 CFR 820.90(a))
and 2 more

Facility details

Company
Retmap Inc
Location
Chicago, IL (US)
Source
device

FDA data resources

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