Home / Facilities / 1000120371

Robert J. Weiss, M.D. — FDA Facility Profile

FEI 1000120371

Robert J. Weiss, M.D. is an FDA-inspected facility (FEI 1000120371) located in Auburn, ME, US. RegDataLab tracks 2 FDA inspections at this facility.

Reviewing Robert J. Weiss, 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 Robert J. Weiss, 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
May 12, 2014: Voluntary Action Indicated (VAI)
Inspections on record
2 (1 VAI, 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
May 12, 2014Voluntary Action Indicated (VAI)Initial and continuing review (21 CFR 312.66)
Case history records- inadequate or inadequate (21 CFR 312.62(b))
FD-1572, protocol compliance (21 CFR 312.60)
Oct 29, 2013No Action Indicated (NAI)No citations listed

Facility details

Company
Robert J. Weiss, M.D.
Location
Auburn, ME (US)
Source
inspections

FDA data resources

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