FDA inspection

HTL-STREFA S.A.: FDA inspection ending Dec 14, 2017

FDA inspection 1038529 · No Action Indicated (NAI) · Ozorkow

Key facts

Inspection ID 1038529
Firm HTL-STREFA S.A.
FEI number 3004034544
Address Ul. Adamowek 7
City Ozorkow
Country Poland
Fiscal year 2018
Inspection end date Dec 14, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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