What does 482 mean?
482 means FDA form for notice of inspection
What is the abbreviation for FDA form for notice of inspection?
FDA form for notice of inspection can be abbreviated as 482
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Most popular questions people look for before coming to this page
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What does 482 stand for? 482 stands for "FDA form for notice of inspection". |
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How to abbreviate "FDA form for notice of inspection"? "FDA form for notice of inspection" can be abbreviated as 482. |
| Q: A: |
What is the meaning of 482 abbreviation? The meaning of 482 abbreviation is "FDA form for notice of inspection". |
| Q: A: |
What is 482 abbreviation? One of the definitions of 482 is "FDA form for notice of inspection". |
| Q: A: |
What does 482 mean? 482 as abbreviation means "FDA form for notice of inspection". |
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What is shorthand of FDA form for notice of inspection? The most common shorthand of "FDA form for notice of inspection" is 482. |
Abbreviations or Slang with similar meaning
- PREINSURV - Prepare for Board of Inspection & Survey
- NOI - Notice of Inspection
- NOOH - Notice of Opportunity for Hearing (first step in FDA procedure to remove a drug from the market against a manufacturer’s desires)
- 1932 - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory
- 1932a - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--voluntary
- 2301 - FDA form for transmittal of periodic reports and promotional material for new animal drugs
- 348 - FDA form for sponsored travel
- 3500 - FDA form for voluntary reporting of adverse events
- 3500A - FDA form for mandatory reporting of adverse events
- 356V - FDA form for new animal drug appication
- 483 - FDA form used as a written notice of deficiencies found in inspections
- FD-1932 - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory
- FD-1932 - FDA form, Veterinary Adverse Drug Reaction, lack of effectiveness, product defect report - Mandatory
- FD-1932a - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report - voluntary
- FD-2301 - FDA form for transmittal of periodic reports and promotional material for new animal drugs
- FD-2301 - FDA form, Transmittal of Periodic Reports and Promotional Material for New Animal Drugs
- FD-356V - FDA form for new animal drug application
- FD-483 - FDA form 483, written notice of deficiencies found in inspections
- FD-483 - FDA form, Written Notice of Deficiencies Found in Inspections
- FORM 482 - Notice Of Inspection