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FDA Inspection
•Levlad, LLC•June 17, 2011

Levlad, LLC – FDA Inspection, Jun 17, 2011

Record Details

This FDA Inspection record concerns Levlad, LLC, with an inspection on June 17, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Levlad, LLC
Inspection Date
June 17, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ace56b26-85ed-43a6-9671-2e407e1aa024

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
732385
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.63Equipment Design, Size and Location
  2. 21 CFR 211.160(b)(4)Establishment of calibration procedures
  3. 21 CFR 211.113(a)Procedures for non-sterile drug products

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Levlad, LLC

6
DateClassificationOfficeProject area
May 19, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 17, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 12, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 13, 2012VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
September 9, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Levlad, LLC
  • FDA Inspection 1171243 - 2022-05-19
  • FDA Inspection 986874 - 2016-08-17
  • FDA Inspection 839430 - 2013-07-12
  • FDA Inspection 791322 - 2012-07-13
  • FDA Inspection 679474 - 2010-09-09

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Contact
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Scranton Office:
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