Data catalog

FDA compliance programs (program assignment codes)

About 67 records

All records

Every FDA compliance program record published by Orca1, 1000 per page. Each page lists the record id and its name; open a record for key facts, related records and what Orca1 adds.

  1. 03037DOMESTIC & IMPORTED CHEESE AND CHEESE PRODUCTS
  2. 03070ADomestic Acidified Food (AF) Products
  3. 03070BDomestic Low-Acid Canned Food (LACF) Products
  4. 03070CDomestic Aseptic Low-Acid Canned Food (LACF) Products
  5. 03836CCOMPREHENSIVE EGG FARM INSPECTIONS/ENVIRONMENTAL SAMPLING
  6. 03844Foodborne Biological Hazards
  7. 03R839RESPONSE TO FOODBORNE EMERGENCIES, NEC
  8. 03R876OEI IMPROVEMENT PROGRAM - FOODS
  9. 03R879SPROUT SAFETY ACTIVITIES
  10. 03R910HFP EXPORT ACTIVITIES
  11. 03S836CTATE CONTRACT COMPREHENSIVE EGG FARM INSPECTIONS/ENVIRONMENTAL SAMPLING
  12. 03S836TSTATE CONTRACT TARGETED EGG FARM INSPECTIONS
  13. 29001DOMESTIC & IMPORT COSMETICS PROGRAM
  14. 29C001CORE COSMETICS INCIDENTS
  15. 41002BINSPECTION OF HCT/PS - 361 REPRODUCTIVE
  16. 41809INSTITUTIONAL REVIEW BOARD (IRB/IRC)
  17. 41B800SHORT TERM ASSIGNMENTS - THERAPEUTIC PRODUCTS - CBER INITIATED
  18. 41R800SHORT TERM ASSIGNMENTS - THERAPEUTIC PRODUCTS - OII HQ/FIELD INITIATED
  19. 42021FARS - CBER-REGULATED PRODUCTS
  20. 42056NDA/ANDA DRUG PROCESS INSPECTIONS (DPI) - CBER-REGULATED PRODUCTS
  21. 42809INSTITUTIONAL REVIEW BOARD (IRB/IRC)
  22. 42B800SHORT TERM ASSIGNMENTS - BLOOD AND BLOOD PRODUCTS - CBER INITIATED
  23. 42R878ZIKA VIRUS ACTIVITIES - BIOLOGICS
  24. 45809INSTITUTIONAL REVIEW BOARD (IRB/IRC)
  25. 45R800SHORT TERM ASSIGNMENTS - VACCINE, ALLERGENIC, AND LIVE BIOTHERAPEUTIC PRODUCTS - OII…
  26. 48809INSTITUTIONAL REVIEW BOARD (IRB/IRC)
  27. 48R800SHORT TERM ASSIGNMENTS - HUMAN DRUGS BIMO - OII HQ/FIELD INITIATED
  28. 52832SPRE-APPROVAL INSPECTIONS - BIOSIMILARS
  29. 56022PDMA - FIELD INITIATED ASSIGNMENTS
  30. 56030ADSCSA - PRODUCT TRACING, VERIFICATION AND SERIALIZATION
  31. 56040Outsourcing Facility Inspection
  32. 56040AAbbreviated Outsourcing Facility Inspection
  33. 56A002MUTUAL RELIANCE HUMAN DRUG GMP INSPECTIONS
  34. 56D015PHARMACY COMPOUNDING ASSIGNMENTS
  35. 56D017503B OUTSOURCING FACILITY ASSIGNMENTS
  36. 63001AHEALTH FRAUD - MISBRANDED DRUGS
  37. 63002NEW DRUGS (RX) W/O APPROVED NDAS
  38. 68001GGeneric Domestic and Foreign PreApproval Inspections, Sample Collections, and Analytical…
  39. 71003AFEED CONTAMINANTS PROGRAM - PESTICIDES/INDUSTRIAL CHEMICALS
  40. 71003BFEED CONTAMINANTS PROGRAM - ELEMENTS
  41. 71003CFEED CONTAMINANTS PROGRAM - MYCOTOXINS
  42. 71006ILLEGAL RESIDUES IN ANIMAL DERIVED FOODS
  43. 71870ANIMAL CELLS, TISSUES, AND CELL- AND TISSUE-BASED PRODUCTS (ACTPS) INSPECTIONS - CVM…
  44. 71R801CONSUMER COMPLAINTS - POST-APPROVAL MONITORING - CVM
  45. 71R839RESPONSE TO ANIMAL FEED EMERGENCIES
  46. 71R853PET FOOD EMERGENCY/RECALL - ANIMAL FOOD USE
  47. 71R876Program 71R876
  48. 71R878FSVP FOREIGN SUPPLIER VERIFICATION PROGRAM - ANIMAL FOODS
  49. 71R881ANIMAL FEED SANITARY TRANSPORTATION INSPECTIONS
  50. 71V023VFD INSPECTION ASSIGNMENTS
  51. 71V026ANIMAL FOOD ENVIRONMENTAL SAMPLING
  52. 71V800SHORT TERM ASSIGNMENTS - CVM INITIATED
  53. 82008MONITORING DEVICES OF FOREIGN ORIGIN
  54. 82818GOVERNMENT WIDE QUALITY ASSURANCE PROGRAM - CDRH
  55. 82845AMEDICAL DEVICE LEVEL I (ABBREVIATED) INSPECTIONS
  56. 82845BMEDICAL DEVICE LEVEL II (BASELINE) INSPECTIONS
  57. 82845CMEDICAL DEVICE LEVEL III (COMPLIANCE FOLLOW-UP) INSPECTIONS
  58. 82R814NATURAL DISASTERS AND EMERGENCIES - MEDICAL DEVICES
  59. 82R833ELECTRONIC ENTRY REVIEW - CDRH MEDICAL DEVICES
  60. 83809INSTITUTIONAL REVIEW BOARD (IRB/IRC)
  61. 83R800SHORT TERM ASSIGNMENTS - OII HQ/FIELD INITIATED
  62. 86003DIAGNOSTIC X-RAY MANUFACTURER COMPLIANCE
  63. 86008MEDICAL DEVICE & RAD HEALTH USE CONTROL POLICY
  64. 96R800SHORT TERM ASSIGNMENTS - OII HQ/FIELD INITIATED
  65. 96T010TOBACCO ABBREVIATED INSPECTIONS
  66. 96T800SHORT TERM ASSIGNMENTS - CTP INITIATED
  67. 98T800SHORT TERM ASSIGNMENTS - CTP INITIATED

About this dataset

FDA inspections and field assignments are planned under compliance programs. Each one is coded with a program assignment code (PAC) that ties it to a program in the FDA Compliance Program Guidance Manual (CPGM).

Source: U.S. Food and Drug Administration (FDA), Compliance Program Guidance Manual and inspection data