FDA inspection

Pristech Products, Inc: FDA inspection ending Sep 9, 2016

FDA inspection 989491 · No Action Indicated (NAI) · San Antonio, TX

Key facts

Inspection ID 989491
Firm Pristech Products, Inc
FEI number 1450530
Address 6952 Fairgrounds Pkwy Ste 107
City San Antonio
State TX
ZIP 78238-4528
Fiscal year 2016
Inspection end date Sep 9, 2016
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes 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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