FDA inspection

Sidmak Laboratories India Pvt Ltd: FDA inspection ending Feb 14, 2020

FDA inspection 1123559 · No Action Indicated (NAI) · Dehradun

Key facts

Inspection ID 1123559
Firm Sidmak Laboratories India Pvt Ltd
FEI number 3008127341
Address Plot No. 20 Pharma City, Selaqui Ind. Area, Vikas Nagar
City Dehradun
Country India
Fiscal year 2020
Inspection end date Feb 14, 2020
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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