Saraca Laboratories Limited - NAI
FDA Inspections Database

Saraca Laboratories Limited - NAI

FDA Inspections Database

U.S. FDA inspection classifications and citation records from the official FDA inspection database.

NAI · No Action Indicated India
  • Total Records 3
  • Latest Inspection 2018-03-22
  • Data Source U.S. FDA
  • Last Updated 2018-05-14

4

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3

NAI
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1

VAI
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Company Overview

Company

Saraca Laboratories Limited - NAI

Country

India

Social Profiles

Company Snapshot

Saraca Laboratories Limited - NAI

Plot No 320, 1st Floor,East Avenue, Swamy Ayyappa Co-Op,Housing Society LTD, Madhapur 500 081

India

www.saraca.com/ info@saraca.com View on Map
FDA Inspections Timeline (3 records)
2018
22 Mar
No Action Indicated NAI

Legal Name

Saraca Laboratories Limited

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2018-03-22

FMD Date

2018-05-14

Fiscal Year

2018

State

Srikakulam, India

Location

Srikakulam, , India

Inspection Info

Fiscal Year: 2018
Citations: No

2015
11 Dec
No Action Indicated NAI

Legal Name

Saraca Laboratories Limited

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2015-12-11

FMD Date

2016-05-02

Fiscal Year

2016

State

Sangareddy, India

Location

Sangareddy, , India

Inspection Info

Fiscal Year: 2016
Citations: No

2013
14 Feb
No Action Indicated NAI

Legal Name

Saraca Laboratories Limited

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2013-02-14

FMD Date

2013-09-25

Fiscal Year

2013

State

Sangareddy, India

Location

Sangareddy, , India

Inspection Info

Fiscal Year: 2013
Citations: No

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Classification Breakdown
3 total
  • NAI (No Action Indicated)
Official Source

All data is sourced from the official FDA inspection database maintained by the U.S. Food and Drug Administration.

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Location

Srikakulam, , India

Inspection Info

Fiscal Year: 2018
Citations: No

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FDA inspection data is compiled from publicly available U.S. FDA inspection classification records.

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