FDA inspection

CutisPharma, Inc.: FDA inspection ending Dec 20, 2017

FDA inspection 1038444 · No Action Indicated (NAI) · Wilmington, MA

Key facts

Inspection ID 1038444
Firm CutisPharma, Inc.
FEI number 3003395329
Address 841 Woburn St
City Wilmington
State MA
ZIP 01887-3414
Fiscal year 2018
Inspection end date Dec 20, 2017
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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