A blank, fillable HACCP plan — cover, product description, hazard analysis, and CCP summary — laid out to FDA's five preliminary tasks and seven principles for you to complete for one product or process.
~30 min
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This is a blank HACCP plan you fill in for one product or one process — not a generic form to file and forget. Reach for it when you are writing your first plan, reworking one an auditor flagged, or finally putting a process you run every day onto paper.
How to use this template
The layout follows FDA's HACCP Principles and Application Guidelines (the NACMCF method, verified July 2026). The five preliminary tasks come first — assemble the team, describe the food and its distribution, describe the intended use, draw the flow diagram, and verify it on the floor — and then the seven principles land in the two tables: the hazard analysis and the CCP summary.
Two terms carry the tables. A is the step you commit to controlling; its is the line it must not cross.
One plan covers one product or process; a facility with several product lines keeps several plans. Fill every blank cell, replace the example rows with your own, and reassess the whole plan at least once a year and whenever an ingredient, process, supplier, or rule changes. Download a blank copy of this template to fill in offline.
Cover
Field
Entry
Facility name
Facility address
Product or product line this plan covers
Plan number and version
Date issued
Next scheduled review
HACCP team
Everyone who owns a piece of the plan. The team should be multidisciplinary — production, sanitation, quality, and people who actually run the line.
Name
Role on the team
Title or department
(example) Dana Ruiz
HACCP coordinator
Quality assurance
Product description and intended use
Preliminary tasks two and three: what the food is, how it moves, who eats it.
Food-safety characteristics (pH, water activity, preservatives)
Packaging
Shelf life and storage conditions
Method of distribution (frozen, refrigerated, ambient)
Intended use and any preparation by the customer
Intended consumers (note any sensitive populations)
Labeling for safe handling and allergens
Process flow
Sketch or attach the flow diagram, then walk the floor to confirm it matches what actually happens. List every step in order, from receiving through shipping.
Receiving — ____
Shipping — ____
Flow diagram verified on the floor by: ____ Date: ____
Hazard analysis
Principle 1. At each step, list every hazard that could be introduced, increased, or controlled there, decide whether it is significant, and name the control.
Process step
Potential hazard — B / C / P
Significant? (Y/N)
Basis for the decision
Control measure
CCP? (Y/N)
(example) Cook
B — pathogen survival (e.g., Salmonella)
Y
Reasonably likely to cause illness with no later kill step
Cook to a validated time and temperature
Y
(example) Weigh and mix
C — undeclared allergen (one of the Big 9)
Y
Allergen-containing products share the line
Allergen control program; label reconciliation
N
(example) Metal detection
P — metal fragment
Y
Equipment wear can shed metal
Functional metal detector on the line
Y
Hazards fall into three families — biological (B), chemical (C), which includes allergens and chemical residues, and physical (P). A hazard is significant when it is reasonably likely to cause injury or illness if it is not controlled — FDA's own test for what belongs in the plan.
Allergens are the Big 9: milk, egg, fish, crustacean shellfish, tree nuts, peanuts, wheat, soybeans, and sesame. Sesame became the ninth major food allergen on January 1, 2023 under the FASTER Act (verified July 2026) — check every product against nine, not eight.
CCP summary
Principles 2 through 7, one row per CCP. These are the columns from FDA's HACCP Plan Summary Table.
CCP
Critical limit(s)
Monitoring (what / how / frequency / who)
Corrective action
Verification
Records
(example) Cook step
Internal temp ≥ ____°F held ≥ ____ min
Probe every batch, recorded by the line lead
Hold or reprocess the affected batch; find and fix the cause
Daily record review; probe calibrated on a set schedule
Cook log; calibration log
Sign-off
The plan is not in force until the people accountable for it sign. Reassess and re-sign at least once a year and after any change to the product, process, ingredients, suppliers, or rules that govern it.